Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154191655G>TCA2695106909OPN1MWc.579-33G>T (n.579-33G>T)
n.588+1433G>T
c.166-33G>T
gnomAD v4
Xg.154191660A>GCA2602677994OPN1MWc.579-28A>G (n.579-28A>G)
n.588+1438A>G
c.166-28A>G
gnomAD v3 gnomAD v4
Xg.154191661G>CCA2695106910OPN1MWc.579-27G>C (n.579-27G>C)
n.588+1439G>C
c.166-27G>C
gnomAD v4
Xg.154191667delCA2739242254OPN1MWc.579-21del (n.579-21del)
n.588+1445del
c.166-21del
dbSNP
Xg.154191667G>CCA2695106911OPN1MWc.579-21G>C (n.579-21G>C)
n.588+1445G>C
c.166-21G>C
gnomAD v4
Xg.154191670G>CCA2466617963OPN1MWc.579-18G>C (n.579-18G>C)
n.588+1448G>C
c.166-18G>C
dbSNP
Xg.154191670G=CA2466617962OPN1MWc.579-18G= (n.579-18G=)
n.588+1448G=
c.166-18G=
Xg.154191672C=CA2466617964OPN1MWc.579-16C= (n.579-16C=)
n.588+1450C=
c.166-16C=
Xg.154191672C>TCA873298043OPN1MWc.579-16C>T (n.579-16C>T)
n.588+1450C>T
c.166-16C>T
dbSNP gnomAD v3 gnomAD v4
Xg.154191673G>ACA2695106912OPN1MWc.579-15G>A (n.579-15G>A)
n.588+1451G>A
c.166-15G>A
gnomAD v4
Xg.154191673G>TCA1138562338OPN1MWc.579-15G>T (n.579-15G>T)
n.588+1451G>T
c.166-15G>T
gnomAD v3 gnomAD v4
Xg.154191674G>ACA1138562339OPN1MWc.579-14G>A (n.579-14G>A)
n.588+1452G>A
c.166-14G>A
gnomAD v3 gnomAD v4
Xg.154191683T>CCA2526450841OPN1MWc.579-5T>C (n.579-5T>C)
n.588+1461T>C
c.166-5T>C
Xg.154191686A>CCA415314617OPN1MWc.579-2A>C (n.579-2A>C)
n.588+1464A>C
c.166-2A>C
Xg.154191686A>GCA415314616OPN1MWc.579-2A>G (n.579-2A>G)
n.588+1464A>G
c.166-2A>G
Xg.154191686A>TCA415314615OPN1MWc.579-2A>T (n.579-2A>T)
n.588+1464A>T
c.166-2A>T
Xg.154191687G>ACA415314618OPN1MWc.579-1G>A (n.579-1G>A)
n.588+1465G>A
c.166-1G>A
Xg.154191687G>CCA415314620OPN1MWc.579-1G>C (n.579-1G>C)
n.588+1465G>C
c.166-1G>C
gnomAD v4
Xg.154191687G>TCA415314619OPN1MWc.579-1G>T (n.579-1G>T)
n.588+1465G>T
c.166-1G>T
Xg.154191688G>ACA519334727OPN1MWc.579G>A (p.Arg193=)
n.588+1466G>A
c.166G>A
Xg.154191688G>CCA415314621OPN1MWc.579G>C (p.Arg193Ser)
n.588+1466G>C
c.166G>C
Xg.154191688G>TCA415314622OPN1MWc.579G>T (p.Arg193Ser)
n.588+1466G>T
c.166G>T
Xg.154191689T>ACA415314623OPN1MWc.580T>A (p.Tyr194Asn)
n.588+1467T>A
c.167T>A
Xg.154191689T>CCA415314625OPN1MWc.580T>C (p.Tyr194His)
n.588+1467T>C
c.167T>C
Xg.154191689T>GCA415314624OPN1MWc.580T>G (p.Tyr194Asp)
n.588+1467T>G
c.167T>G
Xg.154191690A>CCA415314626OPN1MWc.581A>C (p.Tyr194Ser)
n.588+1468A>C
c.168A>C
Xg.154191690A>GCA415314627OPN1MWc.581A>G (p.Tyr194Cys)
n.588+1468A>G
c.168A>G
Xg.154191690A>TCA415314628OPN1MWc.581A>T (p.Tyr194Phe)
n.588+1468A>T
c.168A>T
Xg.154191691C>ACA415314629OPN1MWc.582C>A (p.Tyr194Ter)
n.588+1469C>A
c.169C>A
Xg.154191691C>GCA415314630OPN1MWc.582C>G (p.Tyr194Ter)
n.588+1469C>G
c.169C>G
Xg.154191691C>TCA519334738OPN1MWc.582C>T (p.Tyr194=)
n.588+1469C>T
c.169C>T
Xg.154191692T>ACA415314633OPN1MWc.583T>A (p.Trp195Arg)
n.588+1470T>A
c.170T>A
Xg.154191692T>CCA415314632OPN1MWc.583T>C (p.Trp195Arg)
n.588+1470T>C
c.170T>C
gnomAD v4
Xg.154191692T>GCA415314631OPN1MWc.583T>G (p.Trp195Gly)
n.588+1470T>G
c.170T>G
Xg.154191693G>ACA415314634OPN1MWc.584G>A (p.Trp195Ter)
n.588+1471G>A
c.171G>A
Xg.154191693G>CCA415314635OPN1MWc.584G>C (p.Trp195Ser)
n.588+1471G>C
c.171G>C
Xg.154191693G>TCA415314636OPN1MWc.584G>T (p.Trp195Leu)
n.588+1471G>T
c.171G>T
Xg.154191694G>ACA415314637OPN1MWc.585G>A (p.Trp195Ter)
n.588+1472G>A
c.172G>A
Xg.154191694G>CCA415314638OPN1MWc.585G>C (p.Trp195Cys)
n.588+1472G>C
c.172G>C
Xg.154191694G>TCA415314639OPN1MWc.585G>T (p.Trp195Cys)
n.588+1472G>T
c.172G>T
Xg.154191695C>ACA415314640OPN1MWc.586C>A (p.Pro196Thr)
n.588+1473C>A
c.173C>A
Xg.154191695C>GCA415314642OPN1MWc.586C>G (p.Pro196Ala)
n.588+1473C>G
c.173C>G
Xg.154191695C>TCA415314641OPN1MWc.586C>T (p.Pro196Ser)
n.588+1473C>T
c.173C>T
Xg.154191696C>ACA415314643OPN1MWc.587C>A (p.Pro196His)
n.588+1474C>A
c.174C>A
Xg.154191696C>GCA415314644OPN1MWc.587C>G (p.Pro196Arg)
n.588+1474C>G
c.174C>G
Xg.154191696C>TCA415314645OPN1MWc.587C>T (p.Pro196Leu)
n.588+1474C>T
c.174C>T
Xg.154191697C>ACA519334756OPN1MWc.588C>A (p.Pro196=)
n.588+1475C>A
c.175C>A
Xg.154191697C>GCA519334758OPN1MWc.588C>G (p.Pro196=)
n.588+1475C>G
c.175C>G
Xg.154191697C>TCA519334760OPN1MWc.588C>T (p.Pro196=)
n.588+1475C>T
c.175C>T
Xg.154191698C>ACA415314646OPN1MWc.589C>A (p.His197Asn)
n.588+1476C>A
c.176C>A

Number of alleles fetched