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 |