Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.75196550G>ACA381871148SLCO2B1c.1470G>A (p.Met490Ile)
c.1404G>A (p.Met468Ile)
c.789G>A (p.Met263Ile)
c.1038G>A (p.Met346Ile)
n.276G>A
n.297G>A
n.1017G>A
c.1122G>A (p.Met374Ile)
c.1476G>A (p.Met492Ile)
dbSNP
11g.75196550G>CCA381871149SLCO2B1c.1470G>C (p.Met490Ile)
c.1404G>C (p.Met468Ile)
c.789G>C (p.Met263Ile)
c.1038G>C (p.Met346Ile)
n.276G>C
n.297G>C
n.1017G>C
c.1122G>C (p.Met374Ile)
c.1476G>C (p.Met492Ile)
11g.75196550G=CA1983218005SLCO2B1c.1470G= (p.Met490=)
c.1404G= (p.Met468=)
c.789G= (p.Met263=)
c.1038G= (p.Met346=)
n.276G=
n.297G=
n.1017G=
c.1122G= (p.Met374=)
c.1476G= (p.Met492=)
11g.75196550G>TCA381871150SLCO2B1c.1470G>T (p.Met490Ile)
c.1404G>T (p.Met468Ile)
c.789G>T (p.Met263Ile)
c.1038G>T (p.Met346Ile)
n.276G>T
n.297G>T
n.1017G>T
c.1122G>T (p.Met374Ile)
c.1476G>T (p.Met492Ile)
COSMIC
11g.75196551G>ACA381871151SLCO2B1c.1471G>A (p.Glu491Lys)
c.1405G>A (p.Glu469Lys)
c.790G>A (p.Glu264Lys)
c.1039G>A (p.Glu347Lys)
n.277G>A
n.298G>A
n.1018G>A
c.1123G>A (p.Glu375Lys)
c.1477G>A (p.Glu493Lys)
gnomAD v4
11g.75196551G>CCA381871152SLCO2B1c.1471G>C (p.Glu491Gln)
c.1405G>C (p.Glu469Gln)
c.790G>C (p.Glu264Gln)
c.1039G>C (p.Glu347Gln)
n.277G>C
n.298G>C
n.1018G>C
c.1123G>C (p.Glu375Gln)
c.1477G>C (p.Glu493Gln)
11g.75196551G>TCA381871153SLCO2B1c.1471G>T (p.Glu491Ter)
c.1405G>T (p.Glu469Ter)
c.790G>T (p.Glu264Ter)
c.1039G>T (p.Glu347Ter)
n.277G>T
n.298G>T
n.1018G>T
c.1123G>T (p.Glu375Ter)
c.1477G>T (p.Glu493Ter)
11g.75196552A>CCA381871154SLCO2B1c.1472A>C (p.Glu491Ala)
c.1406A>C (p.Glu469Ala)
c.791A>C (p.Glu264Ala)
c.1040A>C (p.Glu347Ala)
n.278A>C
n.299A>C
n.1019A>C
c.1124A>C (p.Glu375Ala)
c.1478A>C (p.Glu493Ala)
11g.75196552A>GCA381871156SLCO2B1c.1472A>G (p.Glu491Gly)
c.1406A>G (p.Glu469Gly)
c.791A>G (p.Glu264Gly)
c.1040A>G (p.Glu347Gly)
n.278A>G
n.299A>G
n.1019A>G
c.1124A>G (p.Glu375Gly)
c.1478A>G (p.Glu493Gly)
11g.75196552A>TCA381871155SLCO2B1c.1472A>T (p.Glu491Val)
c.1406A>T (p.Glu469Val)
c.791A>T (p.Glu264Val)
c.1040A>T (p.Glu347Val)
n.278A>T
n.299A>T
n.1019A>T
c.1124A>T (p.Glu375Val)
c.1478A>T (p.Glu493Val)
11g.75196553G>ACA475707528SLCO2B1c.1473G>A (p.Glu491=)
c.1407G>A (p.Glu469=)
c.792G>A (p.Glu264=)
c.1041G>A (p.Glu347=)
n.279G>A
n.300G>A
n.1020G>A
c.1125G>A (p.Glu375=)
c.1479G>A (p.Glu493=)
11g.75196553G>CCA381871157SLCO2B1c.1473G>C (p.Glu491Asp)
c.1407G>C (p.Glu469Asp)
c.792G>C (p.Glu264Asp)
c.1041G>C (p.Glu347Asp)
n.279G>C
n.300G>C
n.1020G>C
c.1125G>C (p.Glu375Asp)
c.1479G>C (p.Glu493Asp)
gnomAD v4
11g.75196553G>TCA381871158SLCO2B1c.1473G>T (p.Glu491Asp)
c.1407G>T (p.Glu469Asp)
c.792G>T (p.Glu264Asp)
c.1041G>T (p.Glu347Asp)
n.279G>T
n.300G>T
n.1020G>T
c.1125G>T (p.Glu375Asp)
c.1479G>T (p.Glu493Asp)
11g.75196554G>ACA6188403SLCO2B1c.1474G>A (p.Ala492Thr)
c.1408G>A (p.Ala470Thr)
c.793G>A (p.Ala265Thr)
c.1042G>A (p.Ala348Thr)
n.280G>A
n.301G>A
n.1021G>A
c.1126G>A (p.Ala376Thr)
c.1480G>A (p.Ala494Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.75196554G>CCA381871159SLCO2B1c.1474G>C (p.Ala492Pro)
c.1408G>C (p.Ala470Pro)
c.793G>C (p.Ala265Pro)
c.1042G>C (p.Ala348Pro)
n.280G>C
n.301G>C
n.1021G>C
c.1126G>C (p.Ala376Pro)
c.1480G>C (p.Ala494Pro)
dbSNP gnomAD v2 gnomAD v4
11g.75196554G=CA1983218006SLCO2B1c.1474G= (p.Ala492=)
c.1408G= (p.Ala470=)
c.793G= (p.Ala265=)
c.1042G= (p.Ala348=)
n.280G=
n.301G=
n.1021G=
c.1126G= (p.Ala376=)
c.1480G= (p.Ala494=)
11g.75196554G>TCA381871160SLCO2B1c.1474G>T (p.Ala492Ser)
c.1408G>T (p.Ala470Ser)
c.793G>T (p.Ala265Ser)
c.1042G>T (p.Ala348Ser)
n.280G>T
n.301G>T
n.1021G>T
c.1126G>T (p.Ala376Ser)
c.1480G>T (p.Ala494Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.75196555C>ACA381871161SLCO2B1c.1475C>A (p.Ala492Asp)
c.1409C>A (p.Ala470Asp)
c.794C>A (p.Ala265Asp)
c.1043C>A (p.Ala348Asp)
n.281C>A
n.302C>A
n.1022C>A
c.1127C>A (p.Ala376Asp)
c.1481C>A (p.Ala494Asp)
11g.75196555C=CA1983218007SLCO2B1c.1475C= (p.Ala492=)
c.1409C= (p.Ala470=)
c.794C= (p.Ala265=)
c.1043C= (p.Ala348=)
n.281C=
n.302C=
n.1022C=
c.1127C= (p.Ala376=)
c.1481C= (p.Ala494=)
11g.75196555C>GCA381871162SLCO2B1c.1475C>G (p.Ala492Gly)
c.1409C>G (p.Ala470Gly)
c.794C>G (p.Ala265Gly)
c.1043C>G (p.Ala348Gly)
n.281C>G
n.302C>G
n.1022C>G
c.1127C>G (p.Ala376Gly)
c.1481C>G (p.Ala494Gly)
11g.75196555C>TCA381871163SLCO2B1c.1475C>T (p.Ala492Val)
c.1409C>T (p.Ala470Val)
c.794C>T (p.Ala265Val)
c.1043C>T (p.Ala348Val)
n.281C>T
n.302C>T
n.1022C>T
c.1127C>T (p.Ala376Val)
c.1481C>T (p.Ala494Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.75196556C>ACA475707540SLCO2B1c.1476C>A (p.Ala492=)
c.1410C>A (p.Ala470=)
c.795C>A (p.Ala265=)
c.1044C>A (p.Ala348=)
n.282C>A
n.303C>A
n.1023C>A
c.1128C>A (p.Ala376=)
c.1482C>A (p.Ala494=)
11g.75196556C=CA1983218008SLCO2B1c.1476C= (p.Ala492=)
c.1410C= (p.Ala470=)
c.795C= (p.Ala265=)
c.1044C= (p.Ala348=)
n.282C=
n.303C=
n.1023C=
c.1128C= (p.Ala376=)
c.1482C= (p.Ala494=)
11g.75196556C>GCA475707537SLCO2B1c.1476C>G (p.Ala492=)
c.1410C>G (p.Ala470=)
c.795C>G (p.Ala265=)
c.1044C>G (p.Ala348=)
n.282C>G
n.303C>G
n.1023C>G
c.1128C>G (p.Ala376=)
c.1482C>G (p.Ala494=)
11g.75196556C>TCA475707539SLCO2B1c.1476C>T (p.Ala492=)
c.1410C>T (p.Ala470=)
c.795C>T (p.Ala265=)
c.1044C>T (p.Ala348=)
n.282C>T
n.303C>T
n.1023C>T
c.1128C>T (p.Ala376=)
c.1482C>T (p.Ala494=)
dbSNP gnomAD v4
11g.75196557T>ACA381871164SLCO2B1c.1477T>A (p.Cys493Ser)
c.1411T>A (p.Cys471Ser)
c.796T>A (p.Cys266Ser)
c.1045T>A (p.Cys349Ser)
n.283T>A
n.304T>A
n.1024T>A
c.1129T>A (p.Cys377Ser)
c.1483T>A (p.Cys495Ser)
11g.75196557T>CCA381871165SLCO2B1c.1477T>C (p.Cys493Arg)
c.1411T>C (p.Cys471Arg)
c.796T>C (p.Cys266Arg)
c.1045T>C (p.Cys349Arg)
n.283T>C
n.304T>C
n.1024T>C
c.1129T>C (p.Cys377Arg)
c.1483T>C (p.Cys495Arg)
11g.75196557T>GCA381871166SLCO2B1c.1477T>G (p.Cys493Gly)
c.1411T>G (p.Cys471Gly)
c.796T>G (p.Cys266Gly)
c.1045T>G (p.Cys349Gly)
n.283T>G
n.304T>G
n.1024T>G
c.1129T>G (p.Cys377Gly)
c.1483T>G (p.Cys495Gly)
11g.75196558G>ACA381871167SLCO2B1c.1478G>A (p.Cys493Tyr)
c.1412G>A (p.Cys471Tyr)
c.797G>A (p.Cys266Tyr)
c.1046G>A (p.Cys349Tyr)
n.284G>A
n.305G>A
n.1025G>A
c.1130G>A (p.Cys377Tyr)
c.1484G>A (p.Cys495Tyr)
11g.75196558G>CCA381871169SLCO2B1c.1478G>C (p.Cys493Ser)
c.1412G>C (p.Cys471Ser)
c.797G>C (p.Cys266Ser)
c.1046G>C (p.Cys349Ser)
n.284G>C
n.305G>C
n.1025G>C
c.1130G>C (p.Cys377Ser)
c.1484G>C (p.Cys495Ser)
11g.75196558G>TCA381871168SLCO2B1c.1478G>T (p.Cys493Phe)
c.1412G>T (p.Cys471Phe)
c.797G>T (p.Cys266Phe)
c.1046G>T (p.Cys349Phe)
n.284G>T
n.305G>T
n.1025G>T
c.1130G>T (p.Cys377Phe)
c.1484G>T (p.Cys495Phe)
gnomAD v4
11g.75196559C>ACA381871170SLCO2B1c.1479C>A (p.Cys493Ter)
c.1413C>A (p.Cys471Ter)
c.798C>A (p.Cys266Ter)
c.1047C>A (p.Cys349Ter)
n.285C>A
n.306C>A
n.1026C>A
c.1131C>A (p.Cys377Ter)
c.1485C>A (p.Cys495Ter)
11g.75196559C=CA1983218009SLCO2B1c.1479C= (p.Cys493=)
c.1413C= (p.Cys471=)
c.798C= (p.Cys266=)
c.1047C= (p.Cys349=)
n.285C=
n.306C=
n.1026C=
c.1131C= (p.Cys377=)
c.1485C= (p.Cys495=)
11g.75196559C>GCA381871171SLCO2B1c.1479C>G (p.Cys493Trp)
c.1413C>G (p.Cys471Trp)
c.798C>G (p.Cys266Trp)
c.1047C>G (p.Cys349Trp)
n.285C>G
n.306C>G
n.1026C>G
c.1131C>G (p.Cys377Trp)
c.1485C>G (p.Cys495Trp)
11g.75196559C>TCA6188404SLCO2B1c.1479C>T (p.Cys493=)
c.1413C>T (p.Cys471=)
c.798C>T (p.Cys266=)
c.1047C>T (p.Cys349=)
n.285C>T
n.306C>T
n.1026C>T
c.1131C>T (p.Cys377=)
c.1485C>T (p.Cys495=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.75196560T>ACA381871172SLCO2B1c.1480T>A (p.Ser494Thr)
c.1414T>A (p.Ser472Thr)
c.799T>A (p.Ser267Thr)
c.1048T>A (p.Ser350Thr)
n.286T>A
n.307T>A
n.1027T>A
c.1132T>A (p.Ser378Thr)
c.1486T>A (p.Ser496Thr)
11g.75196560T>CCA381871173SLCO2B1c.1480T>C (p.Ser494Pro)
c.1414T>C (p.Ser472Pro)
c.799T>C (p.Ser267Pro)
c.1048T>C (p.Ser350Pro)
n.286T>C
n.307T>C
n.1027T>C
c.1132T>C (p.Ser378Pro)
c.1486T>C (p.Ser496Pro)
11g.75196560T>GCA381871174SLCO2B1c.1480T>G (p.Ser494Ala)
c.1414T>G (p.Ser472Ala)
c.799T>G (p.Ser267Ala)
c.1048T>G (p.Ser350Ala)
n.286T>G
n.307T>G
n.1027T>G
c.1132T>G (p.Ser378Ala)
c.1486T>G (p.Ser496Ala)
11g.75196561C>ACA381871175SLCO2B1c.1481C>A (p.Ser494Tyr)
c.1415C>A (p.Ser472Tyr)
c.800C>A (p.Ser267Tyr)
c.1049C>A (p.Ser350Tyr)
n.287C>A
n.308C>A
n.1028C>A
c.1133C>A (p.Ser378Tyr)
c.1487C>A (p.Ser496Tyr)
11g.75196561C=CA1983218010SLCO2B1c.1481C= (p.Ser494=)
c.1415C= (p.Ser472=)
c.800C= (p.Ser267=)
c.1049C= (p.Ser350=)
n.287C=
n.308C=
n.1028C=
c.1133C= (p.Ser378=)
c.1487C= (p.Ser496=)
11g.75196561C>GCA381871176SLCO2B1c.1481C>G (p.Ser494Cys)
c.1415C>G (p.Ser472Cys)
c.800C>G (p.Ser267Cys)
c.1049C>G (p.Ser350Cys)
n.287C>G
n.308C>G
n.1028C>G
c.1133C>G (p.Ser378Cys)
c.1487C>G (p.Ser496Cys)
11g.75196561C>TCA6188405SLCO2B1c.1481C>T (p.Ser494Phe)
c.1415C>T (p.Ser472Phe)
c.800C>T (p.Ser267Phe)
c.1049C>T (p.Ser350Phe)
n.287C>T
n.308C>T
n.1028C>T
c.1133C>T (p.Ser378Phe)
c.1487C>T (p.Ser496Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.75196562C>ACA475707558SLCO2B1c.1482C>A (p.Ser494=)
c.1416C>A (p.Ser472=)
c.801C>A (p.Ser267=)
c.1050C>A (p.Ser350=)
n.288C>A
n.309C>A
n.1029C>A
c.1134C>A (p.Ser378=)
c.1488C>A (p.Ser496=)
11g.75196562C>GCA475707560SLCO2B1c.1482C>G (p.Ser494=)
c.1416C>G (p.Ser472=)
c.801C>G (p.Ser267=)
c.1050C>G (p.Ser350=)
n.288C>G
n.309C>G
n.1029C>G
c.1134C>G (p.Ser378=)
c.1488C>G (p.Ser496=)
11g.75196562C>TCA475707562SLCO2B1c.1482C>T (p.Ser494=)
c.1416C>T (p.Ser472=)
c.801C>T (p.Ser267=)
c.1050C>T (p.Ser350=)
n.288C>T
n.309C>T
n.1029C>T
c.1134C>T (p.Ser378=)
c.1488C>T (p.Ser496=)
11g.75196563T>ACA381871179SLCO2B1c.1483T>A (p.Cys495Ser)
c.1417T>A (p.Cys473Ser)
c.802T>A (p.Cys268Ser)
c.1051T>A (p.Cys351Ser)
n.289T>A
n.310T>A
n.1030T>A
c.1135T>A (p.Cys379Ser)
c.1489T>A (p.Cys497Ser)
11g.75196563T>CCA381871177SLCO2B1c.1483T>C (p.Cys495Arg)
c.1417T>C (p.Cys473Arg)
c.802T>C (p.Cys268Arg)
c.1051T>C (p.Cys351Arg)
n.289T>C
n.310T>C
n.1030T>C
c.1135T>C (p.Cys379Arg)
c.1489T>C (p.Cys497Arg)
11g.75196563T>GCA381871178SLCO2B1c.1483T>G (p.Cys495Gly)
c.1417T>G (p.Cys473Gly)
c.802T>G (p.Cys268Gly)
c.1051T>G (p.Cys351Gly)
n.289T>G
n.310T>G
n.1030T>G
c.1135T>G (p.Cys379Gly)
c.1489T>G (p.Cys497Gly)
11g.75196564G>ACA381871180SLCO2B1c.1484G>A (p.Cys495Tyr)
c.1418G>A (p.Cys473Tyr)
c.803G>A (p.Cys268Tyr)
c.1052G>A (p.Cys351Tyr)
n.290G>A
n.311G>A
n.1031G>A
c.1136G>A (p.Cys379Tyr)
c.1490G>A (p.Cys497Tyr)
dbSNP
11g.75196564G>CCA381871181SLCO2B1c.1484G>C (p.Cys495Ser)
c.1418G>C (p.Cys473Ser)
c.803G>C (p.Cys268Ser)
c.1052G>C (p.Cys351Ser)
n.290G>C
n.311G>C
n.1031G>C
c.1136G>C (p.Cys379Ser)
c.1490G>C (p.Cys497Ser)
gnomAD v4

Number of alleles fetched