| SNP | 
                Position | 
                Effect | 
                Amino acid change | 
                   
              
                    
                | C/T | 
                10475439 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/C | 
                10475446 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/G | 
                10475453 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/A | 
                10475463 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10475509 | 
                splice_acceptor_variant&intron_variant | 
                 | 
            
                    
                | G/T | 
                10475529 | 
                synonymous_variant | 
                p.Gly20Gly | 
            
                    
                | G/A | 
                10475594 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/C | 
                10475596 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10475718 | 
                synonymous_variant | 
                p.Thr49Thr | 
            
                    
                | A/T | 
                10475764 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | A/G | 
                10475775 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10475786 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10475825 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10475836 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10475841 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10475850 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G,* | 
                10475957 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10475968 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476001 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10476007 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476055 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G | 
                10476060 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/G | 
                10476067 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476070 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G | 
                10476084 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476087 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/C | 
                10476098 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476201 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476204 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476234 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G,* | 
                10476239 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476243 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10476249 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476250 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476257 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476269 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476316 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10476469 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476506 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10476508 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476531 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G | 
                10476575 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476585 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476600 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/G | 
                10476619 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10476632 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476676 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476680 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/A | 
                10476684 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476705 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476715 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/A | 
                10476727 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476731 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476733 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476753 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10476761 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G | 
                10476780 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476788 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10476792 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476843 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476855 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10476862 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10476880 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10476882 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10476883 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10476889 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10476907 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10476917 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/A | 
                10476920 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10476936 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10476957 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10476992 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477066 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T,* | 
                10477090 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10477106 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10477125 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10477138 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10477256 | 
                missense_variant | 
                p.Ser96Leu | 
            
                    
                | C/T | 
                10477263 | 
                synonymous_variant | 
                p.Ala98Ala | 
            
                    
                | A/T | 
                10477345 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G,* | 
                10477374 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10477379 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | T/C | 
                10477428 | 
                missense_variant | 
                p.Leu122Pro | 
            
                    
                | A/T | 
                10477435 | 
                synonymous_variant | 
                p.Ser124Ser | 
            
                    
                | A/T | 
                10477436 | 
                missense_variant | 
                p.Asn125Tyr | 
            
                    
                | T/C | 
                10477460 | 
                missense_variant | 
                p.Ser133Pro | 
            
                    
                | A/T | 
                10477462 | 
                synonymous_variant | 
                p.Ser133Ser | 
            
                    
                | G/A | 
                10477474 | 
                synonymous_variant | 
                p.Pro137Pro | 
            
                    
                | C/T | 
                10477507 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10477519 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10477523 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10477526 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/A | 
                10477546 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/A | 
                10477550 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10477600 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10477605 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10477617 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10477623 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/A | 
                10477632 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477633 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G | 
                10477651 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477652 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10477659 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10477716 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10477719 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10477723 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/C | 
                10477729 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10477754 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10477766 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/A | 
                10477767 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477771 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477780 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10477810 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10477811 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/T | 
                10477818 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/T | 
                10477895 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477898 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477944 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10477946 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10477960 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/A | 
                10477963 | 
                downstream_gene_variant | 
                 | 
            
                    
                | C/G | 
                10477992 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10478012 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G,C | 
                10478120 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/T | 
                10478163 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/C | 
                10478171 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10478177 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/G | 
                10478193 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | A/G | 
                10478200 | 
                missense_variant&splice_region_variant | 
                p.Thr146Ala | 
            
                    
                | C/T | 
                10478202 | 
                synonymous_variant | 
                p.Thr146Thr | 
            
                    
                | G/C | 
                10478206 | 
                missense_variant | 
                p.Glu148Gln | 
            
                    
                | A/G | 
                10478207 | 
                missense_variant | 
                p.Glu148Gly | 
            
                    
                | G/A | 
                10478236 | 
                missense_variant | 
                p.Glu158Lys | 
            
                    
                | A/C | 
                10478261 | 
                missense_variant | 
                p.Glu166Ala | 
            
                    
                | T/A | 
                10478283 | 
                missense_variant | 
                p.His173Gln | 
            
                    
                | T/C | 
                10478289 | 
                synonymous_variant | 
                p.Tyr175Tyr | 
            
                    
                | C/A | 
                10478366 | 
                stop_gained | 
                p.Ser201* | 
            
                    
                | A/G | 
                10478415 | 
                synonymous_variant | 
                p.Lys217Lys | 
            
                    
                | G/A | 
                10478433 | 
                synonymous_variant | 
                p.Glu223Glu | 
            
                    
                | G/T | 
                10478434 | 
                stop_gained | 
                p.Glu224* | 
            
                    
                | C/T | 
                10478475 | 
                synonymous_variant | 
                p.Ala237Ala | 
            
                    
                | T/C | 
                10478502 | 
                synonymous_variant | 
                p.Leu246Leu | 
            
                    
                | C/T | 
                10478532 | 
                synonymous_variant | 
                p.Val256Val | 
            
                    
                | T/C | 
                10478621 | 
                missense_variant | 
                p.Leu286Ser | 
            
                    
                | A/C | 
                10478639 | 
                missense_variant | 
                p.Lys292Thr | 
            
                    
                | T/C | 
                10478675 | 
                missense_variant | 
                p.Val304Ala | 
            
                    
                | A/G | 
                10478704 | 
                missense_variant&splice_region_variant | 
                p.Arg314Gly | 
            
                    
                | G/A | 
                10478735 | 
                downstream_gene_variant | 
                 | 
            
                    
                | T/C | 
                10478760 | 
                downstream_gene_variant | 
                 | 
            
                    
                | A/C | 
                10478767 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10478791 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/C | 
                10478792 | 
                downstream_gene_variant | 
                 | 
            
                    
                | G/A | 
                10478947 | 
                splice_region_variant&synonymous_variant | 
                p.Arg314Arg | 
            
                    
                | G/A | 
                10479019 | 
                synonymous_variant | 
                p.Thr338Thr | 
            
                    
                | G/C,* | 
                10479024 | 
                missense_variant | 
                p.Arg340Thr | 
            
                    
                | A/T | 
                10479026 | 
                stop_gained | 
                p.Lys341* | 
            
                    
                | C/T | 
                10479044 | 
                stop_gained | 
                p.Gln347* | 
            
                    
                | A/T | 
                10479132 | 
                missense_variant | 
                p.Glu376Val | 
            
                    
                | A/C | 
                10479144 | 
                stop_lost | 
                p.Ter380Serext*? | 
            
                    
                | G/T | 
                10479147 | 
                missense_variant | 
                p.Arg381Leu | 
            
                    
                | T/C | 
                10479169 | 
                synonymous_variant | 
                p.Tyr388Tyr | 
            
                    
                | A/T | 
                10479250 | 
                missense_variant | 
                p.Lys415Asn | 
            
                    
                | A/G | 
                10479253 | 
                stop_retained_variant | 
                p.Ter416Ter | 
            
                    
                | C/T | 
                10479261 | 
                missense_variant | 
                p.Ser419Phe | 
            
                    
                | C/A | 
                10479334 | 
                stop_gained | 
                p.Tyr443* | 
            
                    
                | A/T | 
                10479341 | 
                missense_variant | 
                p.Thr446Ser | 
            
                    
                | T/C | 
                10479360 | 
                missense_variant | 
                p.Leu452Ser | 
            
                    
                | C/T | 
                10479390 | 
                missense_variant | 
                p.Thr462Ile | 
            
                    
                | T/G | 
                10479443 | 
                stop_lost | 
                p.Ter480Gluext*? | 
            
                    
                | A/C | 
                10479444 | 
                stop_lost | 
                p.Ter480Serext*? | 
            
                    
                | A/T | 
                10479457 | 
                synonymous_variant | 
                p.Thr484Thr | 
            
                    
                | G/A,* | 
                10479459 | 
                stop_gained | 
                p.Trp485* | 
            
                    
                | A/T | 
                10479461 | 
                stop_gained | 
                p.Lys486* | 
            
                    
                | T/A | 
                10479483 | 
                missense_variant | 
                p.Ile493Asn | 
            
                    
                | A/G | 
                10479499 | 
                synonymous_variant | 
                p.Lys498Lys | 
            
                    
                | C/T | 
                10479513 | 
                missense_variant | 
                p.Thr503Ile | 
            
                    
                | C/T | 
                10479568 | 
                synonymous_variant | 
                p.His521His | 
            
                    
                | C/T,A | 
                10479623 | 
                missense_variant | 
                p.Leu540Ile | 
            
                    
                | A/G | 
                10479656 | 
                missense_variant | 
                p.Met551Val | 
            
                    
                | T/G | 
                10479778 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10479847 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10479892 | 
                missense_variant | 
                p.Thr597Ala | 
            
                    
                | G/T | 
                10480065 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10480078 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10480117 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10480120 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10480138 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10480186 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10480187 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10480194 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10480208 | 
                intron_variant | 
                 | 
            
                    
                | C/A | 
                10480313 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10480363 | 
                synonymous_variant | 
                p.Ser610Ser | 
            
                    
                | A/G | 
                10480461 | 
                missense_variant | 
                p.His643Arg | 
            
                    
                | C/A | 
                10480529 | 
                missense_variant | 
                p.Pro666Thr | 
            
                    
                | A/T | 
                10480581 | 
                missense_variant | 
                p.Lys683Ile | 
            
                    
                | G/A | 
                10480599 | 
                missense_variant | 
                p.Ser689Asn | 
            
                    
                | C/T | 
                10480671 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10480738 | 
                synonymous_variant | 
                p.Ser705Ser | 
            
                    
                | G/A | 
                10480981 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10481095 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10481155 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10481185 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10481209 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10481217 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10481225 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10481249 | 
                splice_acceptor_variant&intron_variant | 
                 | 
            
                    
                | A/T | 
                10481253 | 
                missense_variant&splice_region_variant | 
                p.Thr783Ser | 
            
                    
                | T/C | 
                10481272 | 
                missense_variant | 
                p.Phe789Ser | 
            
                    
                | G/A | 
                10481278 | 
                missense_variant | 
                p.Gly791Glu | 
            
                    
                | A/G | 
                10481310 | 
                missense_variant | 
                p.Thr802Ala | 
            
                    
                | A/T | 
                10481328 | 
                stop_gained | 
                p.Lys808* | 
            
                    
                | T/A | 
                10481520 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10481538 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10481567 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10481630 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10481685 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10481731 | 
                intron_variant | 
                 | 
            
                    
                | C/G | 
                10481786 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10481787 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10481801 | 
                splice_acceptor_variant&intron_variant | 
                 | 
            
                    
                | G/A | 
                10481821 | 
                synonymous_variant | 
                p.Val871Val | 
            
                    
                | G/T | 
                10481836 | 
                missense_variant | 
                p.Lys876Asn | 
            
                    
                | G/A | 
                10481865 | 
                stop_gained | 
                p.Trp886* | 
            
                    
                | G/A | 
                10482004 | 
                stop_gained | 
                p.Trp932* | 
            
                    
                | G/A | 
                10482072 | 
                stop_gained | 
                p.Trp955* | 
            
                    
                | G/T | 
                10482138 | 
                missense_variant&splice_region_variant | 
                p.Arg977Met | 
            
                    
                | G/A | 
                10482222 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10482265 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10482269 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10482273 | 
                intron_variant | 
                 | 
            
                    
                | G/C | 
                10482354 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10482404 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10482459 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10482464 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10482483 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10482495 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10482509 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10482515 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10482537 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10482588 | 
                intron_variant | 
                 | 
            
                    
                | C/A | 
                10482605 | 
                intron_variant | 
                 | 
            
                    
                | A/C | 
                10482706 | 
                intron_variant | 
                 | 
            
                    
                | C/T,* | 
                10482743 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10482771 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10482790 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10482867 | 
                intron_variant | 
                 | 
            
                    
                | A/C | 
                10482916 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10482921 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10482922 | 
                intron_variant | 
                 | 
            
                    
                | C/G | 
                10483012 | 
                missense_variant | 
                p.Cys978Trp | 
            
                    
                | C/T | 
                10483071 | 
                missense_variant | 
                p.Thr998Ile | 
            
                    
                | A/T | 
                10483076 | 
                missense_variant | 
                p.Ile1000Phe | 
            
                    
                | C/G | 
                10483096 | 
                missense_variant | 
                p.Asp1006Glu | 
            
                    
                | G/A | 
                10483106 | 
                missense_variant | 
                p.Ala1010Thr | 
            
                    
                | C/T | 
                10483133 | 
                synonymous_variant | 
                p.Leu1019Leu | 
            
                    
                | G/A | 
                10483190 | 
                missense_variant | 
                p.Glu1038Lys | 
            
                    
                | T/A | 
                10483270 | 
                synonymous_variant | 
                p.Pro1064Pro | 
            
                    
                | A/G | 
                10483318 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10483453 | 
                missense_variant | 
                p.Asn1099Asp | 
            
                    
                | G/A | 
                10483506 | 
                synonymous_variant | 
                p.Pro1116Pro | 
            
                    
                | C/G | 
                10483515 | 
                splice_region_variant&synonymous_variant | 
                p.Thr1119Thr | 
            
                    
                | A/G | 
                10483516 | 
                missense_variant&splice_region_variant | 
                p.Ser1120Gly | 
            
                    
                | T/C | 
                10483524 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | T/G | 
                10483526 | 
                intron_variant | 
                 | 
            
                    
                | T/G | 
                10483527 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10483528 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10483546 | 
                intron_variant | 
                 | 
            
                    
                | C/A | 
                10483580 | 
                intron_variant | 
                 | 
            
                    
                | G/T | 
                10483594 | 
                intron_variant | 
                 | 
            
                    
                | T/C,* | 
                10483640 | 
                intron_variant | 
                 | 
            
                    
                | T/C,* | 
                10483646 | 
                intron_variant | 
                 | 
            
                    
                | C/T,* | 
                10483660 | 
                intron_variant | 
                 | 
            
                    
                | C/T,* | 
                10483668 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10483673 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10483674 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10483684 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10483686 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10483714 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10483718 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10483719 | 
                intron_variant | 
                 | 
            
                    
                | C/T,* | 
                10483739 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10483743 | 
                intron_variant | 
                 | 
            
                    
                | A/C | 
                10483767 | 
                intron_variant | 
                 | 
            
                    
                | C/G | 
                10483780 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | A/C | 
                10483844 | 
                missense_variant | 
                p.Lys1140Gln | 
            
                    
                | A/G | 
                10483880 | 
                missense_variant | 
                p.Thr1152Ala | 
            
                    
                | A/T | 
                10483891 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | A/G | 
                10483905 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10483961 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10483993 | 
                missense_variant | 
                p.Val1160Ala | 
            
                    
                | G/A | 
                10483998 | 
                missense_variant | 
                p.Gly1162Arg | 
            
                    
                | T/C | 
                10484010 | 
                missense_variant | 
                p.Tyr1166His | 
            
                    
                | G/T | 
                10484015 | 
                missense_variant | 
                p.Gln1167His | 
            
                    
                | T/A | 
                10484016 | 
                missense_variant | 
                p.Phe1168Ile | 
            
                    
                | A/G | 
                10484020 | 
                missense_variant | 
                p.Asp1169Gly | 
            
                    
                | T/G | 
                10484032 | 
                missense_variant | 
                p.Phe1173Cys | 
            
                    
                | C/A | 
                10484033 | 
                missense_variant | 
                p.Phe1173Leu | 
            
                    
                | C/A | 
                10484046 | 
                synonymous_variant | 
                p.Arg1178Arg | 
            
                    
                | C/T | 
                10484054 | 
                synonymous_variant | 
                p.Ile1180Ile | 
            
                    
                | C/A | 
                10484376 | 
                missense_variant | 
                p.Gln1288Lys | 
            
                    
                | T/C | 
                10484387 | 
                synonymous_variant | 
                p.Phe1291Phe | 
            
                    
                | T/C | 
                10484431 | 
                missense_variant | 
                p.Val1306Ala | 
            
                    
                | C/G | 
                10484433 | 
                missense_variant | 
                p.Leu1307Val | 
            
                    
                | G/A | 
                10484534 | 
                synonymous_variant | 
                p.Lys1340Lys | 
            
                    
                | G/A | 
                10484684 | 
                synonymous_variant | 
                p.Glu1390Glu | 
            
                    
                | G/A | 
                10484701 | 
                missense_variant | 
                p.Gly1396Glu | 
            
                    
                | A/G | 
                10484726 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10484727 | 
                intron_variant | 
                 | 
            
                    
                | C/T,* | 
                10484750 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10484796 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10484809 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10484835 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10484836 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10484896 | 
                intron_variant | 
                 | 
            
                    
                | G/C | 
                10484948 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10484967 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10484974 | 
                intron_variant | 
                 | 
            
                    
                | C/A | 
                10485182 | 
                synonymous_variant | 
                p.Ile1414Ile | 
            
                    
                | G/A | 
                10485188 | 
                synonymous_variant | 
                p.Ala1416Ala | 
            
                    
                | T/G | 
                10485293 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10485467 | 
                stop_gained | 
                p.Arg1473* | 
            
                    
                | G/T,* | 
                10485502 | 
                missense_variant | 
                p.Glu1484Asp | 
            
                    
                | C/G | 
                10485661 | 
                missense_variant | 
                p.Asp1537Glu | 
            
                    
                | C/T | 
                10485680 | 
                synonymous_variant | 
                p.Leu1544Leu | 
            
                    
                | T/C | 
                10485763 | 
                synonymous_variant | 
                p.Val1571Val | 
            
                    
                | C/T | 
                10485774 | 
                missense_variant | 
                p.Ser1575Leu | 
            
                    
                | G/A | 
                10485790 | 
                synonymous_variant | 
                p.Leu1580Leu | 
            
                    
                | T/A | 
                10485849 | 
                missense_variant | 
                p.Ile1600Lys | 
            
                    
                | C/A | 
                10485860 | 
                missense_variant | 
                p.Pro1604Thr | 
            
                    
                | T/C | 
                10485866 | 
                missense_variant | 
                p.Cys1606Arg | 
            
                    
                | C/T | 
                10485969 | 
                missense_variant | 
                p.Ser1640Phe | 
            
                    
                | G/C | 
                10485987 | 
                missense_variant | 
                p.Gly1646Ala | 
            
                    
                | A/C | 
                10486006 | 
                synonymous_variant | 
                p.Ser1652Ser | 
            
                    
                | G/C | 
                10486014 | 
                missense_variant | 
                p.Ser1655Thr | 
            
                    
                | G/T | 
                10486089 | 
                missense_variant | 
                p.Cys1680Phe | 
            
                    
                | C/G | 
                10486111 | 
                missense_variant | 
                p.Phe1687Leu | 
            
                    
                | C/T | 
                10486112 | 
                missense_variant | 
                p.His1688Tyr | 
            
                    
                | C/A | 
                10486142 | 
                missense_variant | 
                p.Leu1698Ile | 
            
                    
                | T/C | 
                10486148 | 
                missense_variant | 
                p.Ser1700Pro | 
            
                    
                | A/G | 
                10486193 | 
                missense_variant | 
                p.Asn1715Asp | 
            
                    
                | T/C | 
                10486254 | 
                missense_variant | 
                p.Leu1735Ser | 
            
                    
                | T/A | 
                10486283 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10486308 | 
                intron_variant | 
                 | 
            
                    
                | T/C | 
                10486325 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10486331 | 
                intron_variant | 
                 | 
            
                    
                | T/A | 
                10486332 | 
                intron_variant | 
                 | 
            
                    
                | C/T | 
                10486455 | 
                missense_variant | 
                p.Thr1751Ile | 
            
                    
                | T/A | 
                10486477 | 
                synonymous_variant | 
                p.Ser1758Ser | 
            
                    
                | A/G | 
                10486488 | 
                missense_variant | 
                p.Asn1762Ser | 
            
                    
                | T/C | 
                10486497 | 
                missense_variant | 
                p.Phe1765Ser | 
            
                    
                | A/C | 
                10486503 | 
                missense_variant | 
                p.Glu1767Ala | 
            
                    
                | C/G | 
                10486520 | 
                missense_variant | 
                p.Gln1773Glu | 
            
                    
                | G/A | 
                10486529 | 
                missense_variant | 
                p.Glu1776Lys | 
            
                    
                | T/C | 
                10486574 | 
                missense_variant | 
                p.Ser1791Pro | 
            
                    
                | T/C | 
                10486576 | 
                synonymous_variant | 
                p.Ser1791Ser | 
            
                    
                | T/A | 
                10486625 | 
                missense_variant | 
                p.Leu1808Ile | 
            
                    
                | A/C | 
                10486714 | 
                splice_region_variant&intron_variant | 
                 | 
            
                    
                | G/T | 
                10486770 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10486776 | 
                intron_variant | 
                 | 
            
                    
                | G/A | 
                10486802 | 
                intron_variant | 
                 | 
            
                    
                | A/T | 
                10486816 | 
                intron_variant | 
                 | 
            
                    
                | A/G | 
                10486826 | 
                intron_variant | 
                 | 
            
                    
                | T/G | 
                10486845 | 
                missense_variant&splice_region_variant | 
                p.His1837Gln | 
            
                    
                | G/A | 
                10486859 | 
                missense_variant | 
                p.Gly1842Glu | 
            
                    
                | T/C | 
                10486896 | 
                synonymous_variant | 
                p.Asn1854Asn | 
            
                    
                | C/G | 
                10486977 | 
                missense_variant | 
                p.Asn1881Lys | 
            
                    
                | C/A | 
                10487021 | 
                missense_variant | 
                p.Pro1896Gln | 
            
                    
                | C/T | 
                10487075 | 
                missense_variant | 
                p.Ser1914Phe | 
            
                    
                | C/G | 
                10487113 | 
                missense_variant | 
                p.Arg1927Gly | 
            
                    
                | T/C | 
                10487115 | 
                synonymous_variant | 
                p.Arg1927Arg |