Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.125317600C>ACA358117378FAT4c.1189C>A (p.Gln397Lys)
c.-55+1623C>A (n.-55+1623C>A)
4g.125317600C>GCA358117379FAT4c.1189C>G (p.Gln397Glu)
c.-55+1623C>G (n.-55+1623C>G)
4g.125317600C>TCA358117380FAT4c.1189C>T (p.Gln397Ter)
c.-55+1623C>T (n.-55+1623C>T)
4g.125317601A=CA1491600257FAT4c.1190A= (p.Gln397=)
c.-55+1624A= (n.-55+1624A=)
4g.125317601A>CCA358117382FAT4c.1190A>C (p.Gln397Pro)
c.-55+1624A>C (n.-55+1624A>C)
4g.125317601A>GCA3071938FAT4c.1190A>G (p.Gln397Arg)
c.-55+1624A>G (n.-55+1624A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317601A>TCA358117381FAT4c.1190A>T (p.Gln397Leu)
c.-55+1624A>T (n.-55+1624A>T)
4g.125317602A>CCA358117383FAT4c.1191A>C (p.Gln397His)
c.-55+1625A>C (n.-55+1625A>C)
4g.125317602A>GCA441366723FAT4c.1191A>G (p.Gln397=)
c.-55+1625A>G (n.-55+1625A>G)
4g.125317602A>TCA358117384FAT4c.1191A>T (p.Gln397His)
c.-55+1625A>T (n.-55+1625A>T)
4g.125317603A>CCA358117385FAT4c.1192A>C (p.Ile398Leu)
c.-55+1626A>C (n.-55+1626A>C)
4g.125317603A>GCA358117387FAT4c.1192A>G (p.Ile398Val)
c.-55+1626A>G (n.-55+1626A>G)
4g.125317603A>TCA358117386FAT4c.1192A>T (p.Ile398Phe)
c.-55+1626A>T (n.-55+1626A>T)
4g.125317604T>ACA358117388FAT4c.1193T>A (p.Ile398Asn)
c.-55+1627T>A (n.-55+1627T>A)
4g.125317604T>CCA358117389FAT4c.1193T>C (p.Ile398Thr)
c.-55+1627T>C (n.-55+1627T>C)
4g.125317604T>GCA358117390FAT4c.1193T>G (p.Ile398Ser)
c.-55+1627T>G (n.-55+1627T>G)
4g.125317605T>ACA441366732FAT4c.1194T>A (p.Ile398=)
c.-55+1628T>A (n.-55+1628T>A)
4g.125317605T>CCA441366734FAT4c.1194T>C (p.Ile398=)
c.-55+1628T>C (n.-55+1628T>C)
4g.125317605T>GCA358117391FAT4c.1194T>G (p.Ile398Met)
c.-55+1628T>G (n.-55+1628T>G)
4g.125317605_125317606delinsTCCA1491600264FAT4c.1194_1195delinsTC (p.Ile398=)
c.-55+1628_-55+1629delinsTC (n.-55+1628_-55+1629delinsTC)
4g.125317606delCA170763FAT4c.1195del (p.Leu399SerfsTer19)
c.-55+1629del (n.-55+1629del)
ClinVar dbSNP
4g.125317606C>ACA358117392FAT4c.1195C>A (p.Leu399Ile)
c.-55+1629C>A (n.-55+1629C>A)
ClinVar
4g.125317606C>GCA358117393FAT4c.1195C>G (p.Leu399Val)
c.-55+1629C>G (n.-55+1629C>G)
4g.125317606C>TCA358117394FAT4c.1195C>T (p.Leu399Phe)
c.-55+1629C>T (n.-55+1629C>T)
4g.125317607T>ACA358117395FAT4c.1196T>A (p.Leu399His)
c.-55+1630T>A (n.-55+1630T>A)
4g.125317607T>CCA358117396FAT4c.1196T>C (p.Leu399Pro)
c.-55+1630T>C (n.-55+1630T>C)
gnomAD v4
4g.125317607T>GCA358117397FAT4c.1196T>G (p.Leu399Arg)
c.-55+1630T>G (n.-55+1630T>G)
4g.125317608C>ACA441366741FAT4c.1197C>A (p.Leu399=)
c.-55+1631C>A (n.-55+1631C>A)
gnomAD v4
4g.125317608C=CA1491600284FAT4c.1197C= (p.Leu399=)
c.-55+1631C= (n.-55+1631C=)
4g.125317608C>GCA441366739FAT4c.1197C>G (p.Leu399=)
c.-55+1631C>G (n.-55+1631C>G)
4g.125317608C>TCA441366740FAT4c.1197C>T (p.Leu399=)
c.-55+1631C>T (n.-55+1631C>T)
dbSNP gnomAD v2
4g.125317609G>ACA358117399FAT4c.1198G>A (p.Gly400Arg)
c.-55+1632G>A (n.-55+1632G>A)
4g.125317609G>CCA358117398FAT4c.1198G>C (p.Gly400Arg)
c.-55+1632G>C (n.-55+1632G>C)
gnomAD v4
4g.125317609G=CA1491600288FAT4c.1198G= (p.Gly400=)
c.-55+1632G= (n.-55+1632G=)
4g.125317609G>TCA3071939FAT4c.1198G>T (p.Gly400Trp)
c.-55+1632G>T (n.-55+1632G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317610G>ACA358117400FAT4c.1199G>A (p.Gly400Glu)
c.-55+1633G>A (n.-55+1633G>A)
4g.125317610G>CCA358117401FAT4c.1199G>C (p.Gly400Ala)
c.-55+1633G>C (n.-55+1633G>C)
4g.125317610G>TCA358117402FAT4c.1199G>T (p.Gly400Val)
c.-55+1633G>T (n.-55+1633G>T)
4g.125317611G>ACA441366744FAT4c.1200G>A (p.Gly400=)
c.-55+1634G>A (n.-55+1634G>A)
4g.125317611G>CCA441366745FAT4c.1200G>C (p.Gly400=)
c.-55+1634G>C (n.-55+1634G>C)
4g.125317611G>TCA441366746FAT4c.1200G>T (p.Gly400=)
c.-55+1634G>T (n.-55+1634G>T)
4g.125317612G>ACA358117403FAT4c.1201G>A (p.Gly401Ser)
c.-55+1635G>A (n.-55+1635G>A)
dbSNP gnomAD v3 gnomAD v4
4g.125317612G>CCA358117404FAT4c.1201G>C (p.Gly401Arg)
c.-55+1635G>C (n.-55+1635G>C)
4g.125317612G>TCA358117405FAT4c.1201G>T (p.Gly401Cys)
c.-55+1635G>T (n.-55+1635G>T)
4g.125317613G>ACA358117406FAT4c.1202G>A (p.Gly401Asp)
c.-55+1636G>A (n.-55+1636G>A)
gnomAD v4
4g.125317613G>CCA358117407FAT4c.1202G>C (p.Gly401Ala)
c.-55+1636G>C (n.-55+1636G>C)
4g.125317613G=CA1491600295FAT4c.1202G= (p.Gly401=)
c.-55+1636G= (n.-55+1636G=)
4g.125317613G>TCA3071940FAT4c.1202G>T (p.Gly401Val)
c.-55+1636G>T (n.-55+1636G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317614C>ACA441366750FAT4c.1203C>A (p.Gly401=)
c.-55+1637C>A (n.-55+1637C>A)
4g.125317614C>GCA441366751FAT4c.1203C>G (p.Gly401=)
c.-55+1637C>G (n.-55+1637C>G)
4g.125317614C>TCA441366752FAT4c.1203C>T (p.Gly401=)
c.-55+1637C>T (n.-55+1637C>T)
4g.125317615A>CCA358117408FAT4c.1204A>C (p.Asn402His)
c.-55+1638A>C (n.-55+1638A>C)
4g.125317615A>GCA358117409FAT4c.1204A>G (p.Asn402Asp)
c.-55+1638A>G (n.-55+1638A>G)
4g.125317615A>TCA358117410FAT4c.1204A>T (p.Asn402Tyr)
c.-55+1638A>T (n.-55+1638A>T)
4g.125317616A=CA1491600300FAT4c.1205A= (p.Asn402=)
c.-55+1639A= (n.-55+1639A=)
4g.125317616A>CCA358117413FAT4c.1205A>C (p.Asn402Thr)
c.-55+1639A>C (n.-55+1639A>C)
4g.125317616A>GCA358117412FAT4c.1205A>G (p.Asn402Ser)
c.-55+1639A>G (n.-55+1639A>G)
dbSNP gnomAD v4
4g.125317616A>TCA358117411FAT4c.1205A>T (p.Asn402Ile)
c.-55+1639A>T (n.-55+1639A>T)
4g.125317617T>ACA358117414FAT4c.1206T>A (p.Asn402Lys)
c.-55+1640T>A (n.-55+1640T>A)
4g.125317617T>CCA441366757FAT4c.1206T>C (p.Asn402=)
c.-55+1640T>C (n.-55+1640T>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.125317617T>GCA358117415FAT4c.1206T>G (p.Asn402Lys)
c.-55+1640T>G (n.-55+1640T>G)
gnomAD v4
4g.125317617T=CA1491600303FAT4c.1206T= (p.Asn402=)
c.-55+1640T= (n.-55+1640T=)
4g.125317618G>ACA358117416FAT4c.1207G>A (p.Glu403Lys)
c.-55+1641G>A (n.-55+1641G>A)
4g.125317618G>CCA358117417FAT4c.1207G>C (p.Glu403Gln)
c.-55+1641G>C (n.-55+1641G>C)
4g.125317618G>TCA358117418FAT4c.1207G>T (p.Glu403Ter)
c.-55+1641G>T (n.-55+1641G>T)
4g.125317619A>CCA358117419FAT4c.1208A>C (p.Glu403Ala)
c.-55+1642A>C (n.-55+1642A>C)
4g.125317619A>GCA358117420FAT4c.1208A>G (p.Glu403Gly)
c.-55+1642A>G (n.-55+1642A>G)
4g.125317619A>TCA358117421FAT4c.1208A>T (p.Glu403Val)
c.-55+1642A>T (n.-55+1642A>T)
4g.125317620G>ACA441366763FAT4c.1209G>A (p.Glu403=)
c.-55+1643G>A (n.-55+1643G>A)
4g.125317620G>CCA358117422FAT4c.1209G>C (p.Glu403Asp)
c.-55+1643G>C (n.-55+1643G>C)
4g.125317620G>TCA358117423FAT4c.1209G>T (p.Glu403Asp)
c.-55+1643G>T (n.-55+1643G>T)
4g.125317621C>ACA358117424FAT4c.1210C>A (p.Gln404Lys)
c.-55+1644C>A (n.-55+1644C>A)
4g.125317621C>GCA358117425FAT4c.1210C>G (p.Gln404Glu)
c.-55+1644C>G (n.-55+1644C>G)
4g.125317621C>TCA358117426FAT4c.1210C>T (p.Gln404Ter)
c.-55+1644C>T (n.-55+1644C>T)
4g.125317622A=CA1491600307FAT4c.1211A= (p.Gln404=)
c.-55+1645A= (n.-55+1645A=)
4g.125317622A>CCA3071941FAT4c.1211A>C (p.Gln404Pro)
c.-55+1645A>C (n.-55+1645A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317622A>GCA358117427FAT4c.1211A>G (p.Gln404Arg)
c.-55+1645A>G (n.-55+1645A>G)
4g.125317622A>TCA358117428FAT4c.1211A>T (p.Gln404Leu)
c.-55+1645A>T (n.-55+1645A>T)
4g.125317623G>ACA441366770FAT4c.1212G>A (p.Gln404=)
c.-55+1646G>A (n.-55+1646G>A)
4g.125317623G>CCA358117429FAT4c.1212G>C (p.Gln404His)
c.-55+1646G>C (n.-55+1646G>C)
4g.125317623G=CA1491600312FAT4c.1212G= (p.Gln404=)
c.-55+1646G= (n.-55+1646G=)
4g.125317623G>TCA3071942FAT4c.1212G>T (p.Gln404His)
c.-55+1646G>T (n.-55+1646G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317624C>ACA358117430FAT4c.1213C>A (p.Arg405Ser)
c.-55+1647C>A (n.-55+1647C>A)
4g.125317624C>GCA358117431FAT4c.1213C>G (p.Arg405Gly)
c.-55+1647C>G (n.-55+1647C>G)
4g.125317624C>TCA358117432FAT4c.1213C>T (p.Arg405Cys)
c.-55+1647C>T (n.-55+1647C>T)
4g.125317625G>ACA358117433FAT4c.1214G>A (p.Arg405His)
c.-55+1648G>A (n.-55+1648G>A)
dbSNP COSMIC COSMIC
4g.125317625G>CCA358117434FAT4c.1214G>C (p.Arg405Pro)
c.-55+1648G>C (n.-55+1648G>C)
4g.125317625G=CA1491600317FAT4c.1214G= (p.Arg405=)
c.-55+1648G= (n.-55+1648G=)
4g.125317625G>TCA3071943FAT4c.1214G>T (p.Arg405Leu)
c.-55+1648G>T (n.-55+1648G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317626C>ACA441366778FAT4c.1215C>A (p.Arg405=)
c.-55+1649C>A (n.-55+1649C>A)
4g.125317626C>GCA441366779FAT4c.1215C>G (p.Arg405=)
c.-55+1649C>G (n.-55+1649C>G)
4g.125317626C>TCA441366780FAT4c.1215C>T (p.Arg405=)
c.-55+1649C>T (n.-55+1649C>T)
4g.125317627C>ACA358117435FAT4c.1216C>A (p.His406Asn)
c.-55+1650C>A (n.-55+1650C>A)
4g.125317627C>GCA358117436FAT4c.1216C>G (p.His406Asp)
c.-55+1650C>G (n.-55+1650C>G)
4g.125317627C>TCA358117437FAT4c.1216C>T (p.His406Tyr)
c.-55+1650C>T (n.-55+1650C>T)
4g.125317628A=CA1491600320FAT4c.1217A= (p.His406=)
c.-55+1651A= (n.-55+1651A=)
4g.125317628A>CCA358117440FAT4c.1217A>C (p.His406Pro)
c.-55+1651A>C (n.-55+1651A>C)
4g.125317628A>GCA358117439FAT4c.1217A>G (p.His406Arg)
c.-55+1651A>G (n.-55+1651A>G)
dbSNP gnomAD v4
4g.125317628A>TCA358117438FAT4c.1217A>T (p.His406Leu)
c.-55+1651A>T (n.-55+1651A>T)
4g.125317629C>ACA358117441FAT4c.1218C>A (p.His406Gln)
c.-55+1652C>A (n.-55+1652C>A)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.125317629C=CA1491600326FAT4c.1218C= (p.His406=)
c.-55+1652C= (n.-55+1652C=)
4g.125317629C>GCA358117442FAT4c.1218C>G (p.His406Gln)
c.-55+1652C>G (n.-55+1652C>G)
COSMIC COSMIC
4g.125317629C>TCA441366789FAT4c.1218C>T (p.His406=)
c.-55+1652C>T (n.-55+1652C>T)
ClinVar dbSNP gnomAD v4
4g.125317630T>ACA358117443FAT4c.1219T>A (p.Phe407Ile)
c.-55+1653T>A (n.-55+1653T>A)
4g.125317630T>CCA358117444FAT4c.1219T>C (p.Phe407Leu)
c.-55+1653T>C (n.-55+1653T>C)
ClinVar gnomAD v4
4g.125317630T>GCA358117445FAT4c.1219T>G (p.Phe407Val)
c.-55+1653T>G (n.-55+1653T>G)
4g.125317631T>ACA358117446FAT4c.1220T>A (p.Phe407Tyr)
c.-55+1654T>A (n.-55+1654T>A)
4g.125317631T>CCA358117447FAT4c.1220T>C (p.Phe407Ser)
c.-55+1654T>C (n.-55+1654T>C)
4g.125317631T>GCA358117448FAT4c.1220T>G (p.Phe407Cys)
c.-55+1654T>G (n.-55+1654T>G)
COSMIC COSMIC
4g.125317632T>ACA358117449FAT4c.1221T>A (p.Phe407Leu)
c.-55+1655T>A (n.-55+1655T>A)
4g.125317632T>CCA3071944FAT4c.1221T>C (p.Phe407=)
c.-55+1655T>C (n.-55+1655T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317632T>GCA358117450FAT4c.1221T>G (p.Phe407Leu)
c.-55+1655T>G (n.-55+1655T>G)
4g.125317632T=CA1491600327FAT4c.1221T= (p.Phe407=)
c.-55+1655T= (n.-55+1655T=)
4g.125317633G>ACA3071945FAT4c.1222G>A (p.Glu408Lys)
c.-55+1656G>A (n.-55+1656G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317633G>CCA358117451FAT4c.1222G>C (p.Glu408Gln)
c.-55+1656G>C (n.-55+1656G>C)
4g.125317633G=CA1491600332FAT4c.1222G= (p.Glu408=)
c.-55+1656G= (n.-55+1656G=)
4g.125317633G>TCA358117452FAT4c.1222G>T (p.Glu408Ter)
c.-55+1656G>T (n.-55+1656G>T)
4g.125317634A=CA1491600339FAT4c.1223A= (p.Glu408=)
c.-55+1657A= (n.-55+1657A=)
4g.125317634A>CCA358117454FAT4c.1223A>C (p.Glu408Ala)
c.-55+1657A>C (n.-55+1657A>C)
4g.125317634A>GCA104862029FAT4c.1223A>G (p.Glu408Gly)
c.-55+1657A>G (n.-55+1657A>G)
dbSNP gnomAD v2 gnomAD v4
4g.125317634A>TCA358117453FAT4c.1223A>T (p.Glu408Val)
c.-55+1657A>T (n.-55+1657A>T)
4g.125317635A>CCA358117455FAT4c.1224A>C (p.Glu408Asp)
c.-55+1658A>C (n.-55+1658A>C)
4g.125317635A>GCA441366817FAT4c.1224A>G (p.Glu408=)
c.-55+1658A>G (n.-55+1658A>G)
4g.125317635A>TCA358117456FAT4c.1224A>T (p.Glu408Asp)
c.-55+1658A>T (n.-55+1658A>T)
4g.125317636G>ACA358117457FAT4c.1225G>A (p.Val409Met)
c.-55+1659G>A (n.-55+1659G>A)
gnomAD v4
4g.125317636G>CCA358117458FAT4c.1225G>C (p.Val409Leu)
c.-55+1659G>C (n.-55+1659G>C)
4g.125317636G>TCA358117459FAT4c.1225G>T (p.Val409Leu)
c.-55+1659G>T (n.-55+1659G>T)
4g.125317637T>ACA358117460FAT4c.1226T>A (p.Val409Glu)
c.-55+1660T>A (n.-55+1660T>A)
4g.125317637T>CCA358117461FAT4c.1226T>C (p.Val409Ala)
c.-55+1660T>C (n.-55+1660T>C)
4g.125317637T>GCA358117462FAT4c.1226T>G (p.Val409Gly)
c.-55+1660T>G (n.-55+1660T>G)
4g.125317638G>ACA441366830FAT4c.1227G>A (p.Val409=)
c.-55+1661G>A (n.-55+1661G>A)
4g.125317638G>CCA441366827FAT4c.1227G>C (p.Val409=)
c.-55+1661G>C (n.-55+1661G>C)
4g.125317638G=CA1491600343FAT4c.1227G= (p.Val409=)
c.-55+1661G= (n.-55+1661G=)
4g.125317638G>TCA441366825FAT4c.1227G>T (p.Val409=)
c.-55+1661G>T (n.-55+1661G>T)
ClinVar dbSNP
4g.125317639C>ACA358117463FAT4c.1228C>A (p.Gln410Lys)
c.-55+1662C>A (n.-55+1662C>A)
4g.125317639C>GCA358117464FAT4c.1228C>G (p.Gln410Glu)
c.-55+1662C>G (n.-55+1662C>G)
4g.125317639C>TCA358117465FAT4c.1228C>T (p.Gln410Ter)
c.-55+1662C>T (n.-55+1662C>T)
4g.125317640A>CCA358117467FAT4c.1229A>C (p.Gln410Pro)
c.-55+1663A>C (n.-55+1663A>C)
4g.125317640A>GCA358117468FAT4c.1229A>G (p.Gln410Arg)
c.-55+1663A>G (n.-55+1663A>G)
4g.125317640A>TCA358117466FAT4c.1229A>T (p.Gln410Leu)
c.-55+1663A>T (n.-55+1663A>T)
4g.125317641A=CA1491600349FAT4c.1230A= (p.Gln410=)
c.-55+1664A= (n.-55+1664A=)
4g.125317641A>CCA358117469FAT4c.1230A>C (p.Gln410His)
c.-55+1664A>C (n.-55+1664A>C)
4g.125317641A>GCA441366836FAT4c.1230A>G (p.Gln410=)
c.-55+1664A>G (n.-55+1664A>G)
gnomAD v3 gnomAD v4
4g.125317641A>TCA358117470FAT4c.1230A>T (p.Gln410His)
c.-55+1664A>T (n.-55+1664A>T)
dbSNP gnomAD v2
4g.125317642A>CCA358117471FAT4c.1231A>C (p.Ser411Arg)
c.-55+1665A>C (n.-55+1665A>C)
4g.125317642A>GCA358117472FAT4c.1231A>G (p.Ser411Gly)
c.-55+1665A>G (n.-55+1665A>G)
gnomAD v4
4g.125317642A>TCA358117473FAT4c.1231A>T (p.Ser411Cys)
c.-55+1665A>T (n.-55+1665A>T)
4g.125317643G>ACA358117474FAT4c.1232G>A (p.Ser411Asn)
c.-55+1666G>A (n.-55+1666G>A)
gnomAD v4
4g.125317643G>CCA358117475FAT4c.1232G>C (p.Ser411Thr)
c.-55+1666G>C (n.-55+1666G>C)
4g.125317643G>TCA358117476FAT4c.1232G>T (p.Ser411Ile)
c.-55+1666G>T (n.-55+1666G>T)
4g.125317644C>ACA358117477FAT4c.1233C>A (p.Ser411Arg)
c.-55+1667C>A (n.-55+1667C>A)
4g.125317644C=CA1491600353FAT4c.1233C= (p.Ser411=)
c.-55+1667C= (n.-55+1667C=)
4g.125317644C>GCA358117478FAT4c.1233C>G (p.Ser411Arg)
c.-55+1667C>G (n.-55+1667C>G)
4g.125317644C>TCA441366851FAT4c.1233C>T (p.Ser411=)
c.-55+1667C>T (n.-55+1667C>T)
dbSNP
4g.125317645A>CCA358117479FAT4c.1234A>C (p.Ser412Arg)
c.-55+1668A>C (n.-55+1668A>C)
4g.125317645A>GCA358117480FAT4c.1234A>G (p.Ser412Gly)
c.-55+1668A>G (n.-55+1668A>G)
4g.125317645A>TCA358117481FAT4c.1234A>T (p.Ser412Cys)
c.-55+1668A>T (n.-55+1668A>T)
4g.125317646G>ACA358117484FAT4c.1235G>A (p.Ser412Asn)
c.-55+1669G>A (n.-55+1669G>A)
gnomAD v4
4g.125317646G>CCA358117483FAT4c.1235G>C (p.Ser412Thr)
c.-55+1669G>C (n.-55+1669G>C)
4g.125317646G>TCA358117482FAT4c.1235G>T (p.Ser412Ile)
c.-55+1669G>T (n.-55+1669G>T)
4g.125317647C>ACA358117485FAT4c.1236C>A (p.Ser412Arg)
c.-55+1670C>A (n.-55+1670C>A)
4g.125317647C>GCA358117486FAT4c.1236C>G (p.Ser412Arg)
c.-55+1670C>G (n.-55+1670C>G)
4g.125317647C>TCA441366861FAT4c.1236C>T (p.Ser412=)
c.-55+1670C>T (n.-55+1670C>T)
4g.125317648A=CA1491600358FAT4c.1237A= (p.Lys413=)
c.-55+1671A= (n.-55+1671A=)
4g.125317648A>CCA358117487FAT4c.1237A>C (p.Lys413Gln)
c.-55+1671A>C (n.-55+1671A>C)
4g.125317648A>GCA358117488FAT4c.1237A>G (p.Lys413Glu)
c.-55+1671A>G (n.-55+1671A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.125317648A>TCA358117489FAT4c.1237A>T (p.Lys413Ter)
c.-55+1671A>T (n.-55+1671A>T)
4g.125317649A>CCA358117490FAT4c.1238A>C (p.Lys413Thr)
c.-55+1672A>C (n.-55+1672A>C)
4g.125317649A>GCA358117491FAT4c.1238A>G (p.Lys413Arg)
c.-55+1672A>G (n.-55+1672A>G)
4g.125317649A>TCA358117492FAT4c.1238A>T (p.Lys413Ile)
c.-55+1672A>T (n.-55+1672A>T)
4g.125317650A>CCA358117493FAT4c.1239A>C (p.Lys413Asn)
c.-55+1673A>C (n.-55+1673A>C)
4g.125317650A>GCA441366875FAT4c.1239A>G (p.Lys413=)
c.-55+1673A>G (n.-55+1673A>G)
4g.125317650A>TCA358117494FAT4c.1239A>T (p.Lys413Asn)
c.-55+1673A>T (n.-55+1673A>T)
4g.125317651G>ACA358117495FAT4c.1240G>A (p.Val414Met)
c.-55+1674G>A (n.-55+1674G>A)
4g.125317651G>CCA358117496FAT4c.1240G>C (p.Val414Leu)
c.-55+1674G>C (n.-55+1674G>C)
gnomAD v4
4g.125317651G>TCA358117497FAT4c.1240G>T (p.Val414Leu)
c.-55+1674G>T (n.-55+1674G>T)
4g.125317652T>ACA358117499FAT4c.1241T>A (p.Val414Glu)
c.-55+1675T>A (n.-55+1675T>A)
4g.125317652T>CCA3071946FAT4c.1241T>C (p.Val414Ala)
c.-55+1675T>C (n.-55+1675T>C)
dbSNP ExAC gnomAD v2
4g.125317652T>GCA358117498FAT4c.1241T>G (p.Val414Gly)
c.-55+1675T>G (n.-55+1675T>G)
4g.125317652T=CA1491600364FAT4c.1241T= (p.Val414=)
c.-55+1675T= (n.-55+1675T=)
4g.125317653G>ACA441366887FAT4c.1242G>A (p.Val414=)
c.-55+1676G>A (n.-55+1676G>A)
4g.125317653G>CCA441366889FAT4c.1242G>C (p.Val414=)
c.-55+1676G>C (n.-55+1676G>C)
4g.125317653G>TCA441366890FAT4c.1242G>T (p.Val414=)
c.-55+1676G>T (n.-55+1676G>T)
4g.125317654C>ACA358117501FAT4c.1243C>A (p.Pro415Thr)
c.-55+1677C>A (n.-55+1677C>A)
4g.125317654C>GCA358117500FAT4c.1243C>G (p.Pro415Ala)
c.-55+1677C>G (n.-55+1677C>G)
4g.125317654C>TCA358117502FAT4c.1243C>T (p.Pro415Ser)
c.-55+1677C>T (n.-55+1677C>T)
gnomAD v4 COSMIC COSMIC
4g.125317655C>ACA358117503FAT4c.1244C>A (p.Pro415Gln)
c.-55+1678C>A (n.-55+1678C>A)
4g.125317655C=CA1491600368FAT4c.1244C= (p.Pro415=)
c.-55+1678C= (n.-55+1678C=)
4g.125317655C>GCA3071947FAT4c.1244C>G (p.Pro415Arg)
c.-55+1678C>G (n.-55+1678C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317655C>TCA104862065FAT4c.1244C>T (p.Pro415Leu)
c.-55+1678C>T (n.-55+1678C>T)
dbSNP
4g.125317656G>ACA441366900FAT4c.1245G>A (p.Pro415=)
c.-55+1679G>A (n.-55+1679G>A)
dbSNP COSMIC COSMIC
4g.125317656G>CCA441366901FAT4c.1245G>C (p.Pro415=)
c.-55+1679G>C (n.-55+1679G>C)
4g.125317656G=CA1491600376FAT4c.1245G= (p.Pro415=)
c.-55+1679G= (n.-55+1679G=)
4g.125317656G>TCA441366902FAT4c.1245G>T (p.Pro415=)
c.-55+1679G>T (n.-55+1679G>T)
ClinVar dbSNP gnomAD v4
4g.125317657A>CCA358117504FAT4c.1246A>C (p.Asn416His)
c.-55+1680A>C (n.-55+1680A>C)
4g.125317657A>GCA358117506FAT4c.1246A>G (p.Asn416Asp)
c.-55+1680A>G (n.-55+1680A>G)
4g.125317657A>TCA358117505FAT4c.1246A>T (p.Asn416Tyr)
c.-55+1680A>T (n.-55+1680A>T)
4g.125317658A>CCA358117507FAT4c.1247A>C (p.Asn416Thr)
c.-55+1681A>C (n.-55+1681A>C)
4g.125317658A>GCA358117508FAT4c.1247A>G (p.Asn416Ser)
c.-55+1681A>G (n.-55+1681A>G)
4g.125317658A>TCA358117509FAT4c.1247A>T (p.Asn416Ile)
c.-55+1681A>T (n.-55+1681A>T)
4g.125317659C>ACA358117510FAT4c.1248C>A (p.Asn416Lys)
c.-55+1682C>A (n.-55+1682C>A)
4g.125317659C=CA1491600381FAT4c.1248C= (p.Asn416=)
c.-55+1682C= (n.-55+1682C=)
4g.125317659C>GCA358117511FAT4c.1248C>G (p.Asn416Lys)
c.-55+1682C>G (n.-55+1682C>G)
4g.125317659C>TCA3071948FAT4c.1248C>T (p.Asn416=)
c.-55+1682C>T (n.-55+1682C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317660C>ACA358117512FAT4c.1249C>A (p.Leu417Met)
c.-55+1683C>A (n.-55+1683C>A)
4g.125317660C=CA1491600394FAT4c.1249C= (p.Leu417=)
c.-55+1683C= (n.-55+1683C=)
4g.125317660C>GCA358117513FAT4c.1249C>G (p.Leu417Val)
c.-55+1683C>G (n.-55+1683C>G)
4g.125317660C>TCA441366916FAT4c.1249C>T (p.Leu417=)
c.-55+1683C>T (n.-55+1683C>T)
dbSNP
4g.125317661T>ACA358117514FAT4c.1250T>A (p.Leu417Gln)
c.-55+1684T>A (n.-55+1684T>A)
4g.125317661T>CCA358117515FAT4c.1250T>C (p.Leu417Pro)
c.-55+1684T>C (n.-55+1684T>C)
dbSNP
4g.125317661T>GCA358117516FAT4c.1250T>G (p.Leu417Arg)
c.-55+1684T>G (n.-55+1684T>G)
4g.125317661T=CA1491600403FAT4c.1250T= (p.Leu417=)
c.-55+1684T= (n.-55+1684T=)
4g.125317662G>ACA441366922FAT4c.1251G>A (p.Leu417=)
c.-55+1685G>A (n.-55+1685G>A)
4g.125317662G>CCA441366920FAT4c.1251G>C (p.Leu417=)
c.-55+1685G>C (n.-55+1685G>C)
4g.125317662G>TCA441366918FAT4c.1251G>T (p.Leu417=)
c.-55+1685G>T (n.-55+1685G>T)
4g.125317663A=CA1491600407FAT4c.1252A= (p.Ser418=)
c.-55+1686A= (n.-55+1686A=)
4g.125317663A>CCA358117519FAT4c.1252A>C (p.Ser418Arg)
c.-55+1686A>C (n.-55+1686A>C)
4g.125317663A>GCA358117518FAT4c.1252A>G (p.Ser418Gly)
c.-55+1686A>G (n.-55+1686A>G)
4g.125317663A>TCA358117517FAT4c.1252A>T (p.Ser418Cys)
c.-55+1686A>T (n.-55+1686A>T)
dbSNP
4g.125317664G>ACA358117520FAT4c.1253G>A (p.Ser418Asn)
c.-55+1687G>A (n.-55+1687G>A)
4g.125317664G>CCA104862100FAT4c.1253G>C (p.Ser418Thr)
c.-55+1687G>C (n.-55+1687G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.125317664G=CA1491600418FAT4c.1253G= (p.Ser418=)
c.-55+1687G= (n.-55+1687G=)
4g.125317664G>TCA358117521FAT4c.1253G>T (p.Ser418Ile)
c.-55+1687G>T (n.-55+1687G>T)
dbSNP gnomAD v2 gnomAD v4
4g.125317665C>ACA358117522FAT4c.1254C>A (p.Ser418Arg)
c.-55+1688C>A (n.-55+1688C>A)
4g.125317665C=CA1491600426FAT4c.1254C= (p.Ser418=)
c.-55+1688C= (n.-55+1688C=)
4g.125317665C>GCA358117523FAT4c.1254C>G (p.Ser418Arg)
c.-55+1688C>G (n.-55+1688C>G)
4g.125317665C>TCA3071949FAT4c.1254C>T (p.Ser418=)
c.-55+1688C>T (n.-55+1688C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
4g.125317666C>ACA358117524FAT4c.1255C>A (p.Leu419Ile)
c.-55+1689C>A (n.-55+1689C>A)
4g.125317666C>GCA358117525FAT4c.1255C>G (p.Leu419Val)
c.-55+1689C>G (n.-55+1689C>G)
4g.125317666C>TCA441366940FAT4c.1255C>T (p.Leu419=)
c.-55+1689C>T (n.-55+1689C>T)
gnomAD v4
4g.125317667T>ACA358117526FAT4c.1256T>A (p.Leu419Gln)
c.-55+1690T>A (n.-55+1690T>A)
4g.125317667T>CCA358117527FAT4c.1256T>C (p.Leu419Pro)
c.-55+1690T>C (n.-55+1690T>C)
COSMIC COSMIC
4g.125317667T>GCA358117528FAT4c.1256T>G (p.Leu419Arg)
c.-55+1690T>G (n.-55+1690T>G)
4g.125317668A=CA1491600436FAT4c.1257A= (p.Leu419=)
c.-55+1691A= (n.-55+1691A=)
4g.125317668A>CCA441366943FAT4c.1257A>C (p.Leu419=)
c.-55+1691A>C (n.-55+1691A>C)
dbSNP gnomAD v3 gnomAD v4
4g.125317668A>GCA441366945FAT4c.1257A>G (p.Leu419=)
c.-55+1691A>G (n.-55+1691A>G)
gnomAD v4
4g.125317668A>TCA441366944FAT4c.1257A>T (p.Leu419=)
c.-55+1691A>T (n.-55+1691A>T)
4g.125317669A>CCA358117531FAT4c.1258A>C (p.Ile420Leu)
c.-55+1692A>C (n.-55+1692A>C)
4g.125317669A>GCA358117530FAT4c.1258A>G (p.Ile420Val)
c.-55+1692A>G (n.-55+1692A>G)
ClinVar dbSNP gnomAD v4
4g.125317669A>TCA358117529FAT4c.1258A>T (p.Ile420Phe)
c.-55+1692A>T (n.-55+1692A>T)
4g.125317670T>ACA358117532FAT4c.1259T>A (p.Ile420Asn)
c.-55+1693T>A (n.-55+1693T>A)
4g.125317670T>CCA358117533FAT4c.1259T>C (p.Ile420Thr)
c.-55+1693T>C (n.-55+1693T>C)
4g.125317670T>GCA358117534FAT4c.1259T>G (p.Ile420Ser)
c.-55+1693T>G (n.-55+1693T>G)
4g.125317671C>ACA441366947FAT4c.1260C>A (p.Ile420=)
c.-55+1694C>A (n.-55+1694C>A)
4g.125317671C=CA1491600440FAT4c.1260C= (p.Ile420=)
c.-55+1694C= (n.-55+1694C=)
4g.125317671C>GCA358117535FAT4c.1260C>G (p.Ile420Met)
c.-55+1694C>G (n.-55+1694C>G)
4g.125317671C>TCA441366955FAT4c.1260C>T (p.Ile420=)
c.-55+1694C>T (n.-55+1694C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.125317672A>CCA358117536FAT4c.1261A>C (p.Lys421Gln)
c.-55+1695A>C (n.-55+1695A>C)
4g.125317672A>GCA358117537FAT4c.1261A>G (p.Lys421Glu)
c.-55+1695A>G (n.-55+1695A>G)
4g.125317672A>TCA358117538FAT4c.1261A>T (p.Lys421Ter)
c.-55+1695A>T (n.-55+1695A>T)
4g.125317673A>CCA358117539FAT4c.1262A>C (p.Lys421Thr)
c.-55+1696A>C (n.-55+1696A>C)
ClinVar
4g.125317673A>GCA358117540FAT4c.1262A>G (p.Lys421Arg)
c.-55+1696A>G (n.-55+1696A>G)
4g.125317673A>TCA358117541FAT4c.1262A>T (p.Lys421Met)
c.-55+1696A>T (n.-55+1696A>T)
4g.125317674G>ACA441366969FAT4c.1263G>A (p.Lys421=)
c.-55+1697G>A (n.-55+1697G>A)
4g.125317674G>CCA358117542FAT4c.1263G>C (p.Lys421Asn)
c.-55+1697G>C (n.-55+1697G>C)
4g.125317674G>TCA358117543FAT4c.1263G>T (p.Lys421Asn)
c.-55+1697G>T (n.-55+1697G>T)
4g.125317675G>ACA3071950FAT4c.1264G>A (p.Val422Met)
c.-55+1698G>A (n.-55+1698G>A)
dbSNP ExAC gnomAD v2
4g.125317675G>CCA358117545FAT4c.1264G>C (p.Val422Leu)
c.-55+1698G>C (n.-55+1698G>C)
4g.125317675G=CA1491600445FAT4c.1264G= (p.Val422=)
c.-55+1698G= (n.-55+1698G=)
4g.125317675G>TCA358117544FAT4c.1264G>T (p.Val422Leu)
c.-55+1698G>T (n.-55+1698G>T)
gnomAD v4
4g.125317676T>ACA358117546FAT4c.1265T>A (p.Val422Glu)
c.-55+1699T>A (n.-55+1699T>A)
4g.125317676T>CCA358117547FAT4c.1265T>C (p.Val422Ala)
c.-55+1699T>C (n.-55+1699T>C)
dbSNP gnomAD v4
4g.125317676T>GCA358117548FAT4c.1265T>G (p.Val422Gly)
c.-55+1699T>G (n.-55+1699T>G)
4g.125317676T=CA1491600450FAT4c.1265T= (p.Val422=)
c.-55+1699T= (n.-55+1699T=)
4g.125317677G>ACA441366975FAT4c.1266G>A (p.Val422=)
c.-55+1700G>A (n.-55+1700G>A)
4g.125317677G>CCA441366977FAT4c.1266G>C (p.Val422=)
c.-55+1700G>C (n.-55+1700G>C)
4g.125317677G>TCA441366981FAT4c.1266G>T (p.Val422=)
c.-55+1700G>T (n.-55+1700G>T)
4g.125317678G>ACA358117549FAT4c.1267G>A (p.Ala423Thr)
c.-55+1701G>A (n.-55+1701G>A)
4g.125317678G>CCA358117550FAT4c.1267G>C (p.Ala423Pro)
c.-55+1701G>C (n.-55+1701G>C)
4g.125317678G>TCA358117551FAT4c.1267G>T (p.Ala423Ser)
c.-55+1701G>T (n.-55+1701G>T)
4g.125317679C>ACA358117552FAT4c.1268C>A (p.Ala423Asp)
c.-55+1702C>A (n.-55+1702C>A)
4g.125317679C=CA1491600455FAT4c.1268C= (p.Ala423=)
c.-55+1702C= (n.-55+1702C=)
4g.125317679C>GCA358117553FAT4c.1268C>G (p.Ala423Gly)
c.-55+1702C>G (n.-55+1702C>G)
4g.125317679C>TCA358117554FAT4c.1268C>T (p.Ala423Val)
c.-55+1702C>T (n.-55+1702C>T)
dbSNP gnomAD v2
4g.125317680C>ACA441366987FAT4c.1269C>A (p.Ala423=)
c.-55+1703C>A (n.-55+1703C>A)
4g.125317680C>GCA441366989FAT4c.1269C>G (p.Ala423=)
c.-55+1703C>G (n.-55+1703C>G)
4g.125317680C>TCA441366991FAT4c.1269C>T (p.Ala423=)
c.-55+1703C>T (n.-55+1703C>T)
4g.125317681A>CCA358117555FAT4c.1270A>C (p.Ser424Arg)
c.-55+1704A>C (n.-55+1704A>C)
4g.125317681A>GCA358117556FAT4c.1270A>G (p.Ser424Gly)
c.-55+1704A>G (n.-55+1704A>G)
4g.125317681A>TCA358117557FAT4c.1270A>T (p.Ser424Cys)
c.-55+1704A>T (n.-55+1704A>T)
4g.125317682G>ACA358117560FAT4c.1271G>A (p.Ser424Asn)
c.-55+1705G>A (n.-55+1705G>A)
4g.125317682G>CCA358117559FAT4c.1271G>C (p.Ser424Thr)
c.-55+1705G>C (n.-55+1705G>C)
4g.125317682G>TCA358117558FAT4c.1271G>T (p.Ser424Ile)
c.-55+1705G>T (n.-55+1705G>T)
4g.125317683C>ACA3071951FAT4c.1272C>A (p.Ser424Arg)
c.-55+1706C>A (n.-55+1706C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317683C=CA1491600461FAT4c.1272C= (p.Ser424=)
c.-55+1706C= (n.-55+1706C=)
4g.125317683C>GCA358117561FAT4c.1272C>G (p.Ser424Arg)
c.-55+1706C>G (n.-55+1706C>G)
4g.125317683C>TCA441366997FAT4c.1272C>T (p.Ser424=)
c.-55+1706C>T (n.-55+1706C>T)
gnomAD v4
4g.125317684G>ACA358117562FAT4c.1273G>A (p.Ala425Thr)
c.-55+1707G>A (n.-55+1707G>A)
4g.125317684G>CCA3071952FAT4c.1273G>C (p.Ala425Pro)
c.-55+1707G>C (n.-55+1707G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317684G=CA1491600473FAT4c.1273G= (p.Ala425=)
c.-55+1707G= (n.-55+1707G=)
4g.125317684G>TCA3071953FAT4c.1273G>T (p.Ala425Ser)
c.-55+1707G>T (n.-55+1707G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317685C>ACA358117563FAT4c.1274C>A (p.Ala425Asp)
c.-55+1708C>A (n.-55+1708C>A)
4g.125317685C>GCA358117564FAT4c.1274C>G (p.Ala425Gly)
c.-55+1708C>G (n.-55+1708C>G)
4g.125317685C>TCA358117565FAT4c.1274C>T (p.Ala425Val)
c.-55+1708C>T (n.-55+1708C>T)
4g.125317686C>ACA441367007FAT4c.1275C>A (p.Ala425=)
c.-55+1709C>A (n.-55+1709C>A)
4g.125317686C=CA1491600476FAT4c.1275C= (p.Ala425=)
c.-55+1709C= (n.-55+1709C=)
4g.125317686C>GCA3071954FAT4c.1275C>G (p.Ala425=)
c.-55+1709C>G (n.-55+1709C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317686C>TCA441367008FAT4c.1275C>T (p.Ala425=)
c.-55+1709C>T (n.-55+1709C>T)
ClinVar gnomAD v4
4g.125317687T>ACA358117566FAT4c.1276T>A (p.Leu426Met)
c.-55+1710T>A (n.-55+1710T>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.125317687T>CCA441367011FAT4c.1276T>C (p.Leu426=)
c.-55+1710T>C (n.-55+1710T>C)
dbSNP gnomAD v2 gnomAD v4
4g.125317687T>GCA358117567FAT4c.1276T>G (p.Leu426Val)
c.-55+1710T>G (n.-55+1710T>G)
4g.125317687T=CA1491600482FAT4c.1276T= (p.Leu426=)
c.-55+1710T= (n.-55+1710T=)
4g.125317688T>ACA358117568FAT4c.1277T>A (p.Leu426Ter)
c.-55+1711T>A (n.-55+1711T>A)
4g.125317688T>CCA358117569FAT4c.1277T>C (p.Leu426Ser)
c.-55+1711T>C (n.-55+1711T>C)
4g.125317688T>GCA358117570FAT4c.1277T>G (p.Leu426Trp)
c.-55+1711T>G (n.-55+1711T>G)
4g.125317689G>ACA441367016FAT4c.1278G>A (p.Leu426=)
c.-55+1712G>A (n.-55+1712G>A)
gnomAD v4
4g.125317689G>CCA358117571FAT4c.1278G>C (p.Leu426Phe)
c.-55+1712G>C (n.-55+1712G>C)
4g.125317689G>TCA358117572FAT4c.1278G>T (p.Leu426Phe)
c.-55+1712G>T (n.-55+1712G>T)
4g.125317690G>ACA358117573FAT4c.1279G>A (p.Asp427Asn)
c.-55+1713G>A (n.-55+1713G>A)
4g.125317690G>CCA358117575FAT4c.1279G>C (p.Asp427His)
c.-55+1713G>C (n.-55+1713G>C)
4g.125317690G>TCA358117574FAT4c.1279G>T (p.Asp427Tyr)
c.-55+1713G>T (n.-55+1713G>T)
4g.125317691A>CCA358117576FAT4c.1280A>C (p.Asp427Ala)
c.-55+1714A>C (n.-55+1714A>C)
4g.125317691A>GCA358117577FAT4c.1280A>G (p.Asp427Gly)
c.-55+1714A>G (n.-55+1714A>G)
4g.125317691A>TCA358117578FAT4c.1280A>T (p.Asp427Val)
c.-55+1714A>T (n.-55+1714A>T)
4g.125317692C>ACA358117579FAT4c.1281C>A (p.Asp427Glu)
c.-55+1715C>A (n.-55+1715C>A)
gnomAD v4
4g.125317692C=CA1491600484FAT4c.1281C= (p.Asp427=)
c.-55+1715C= (n.-55+1715C=)
4g.125317692C>GCA358117580FAT4c.1281C>G (p.Asp427Glu)
c.-55+1715C>G (n.-55+1715C>G)
dbSNP
4g.125317692C>TCA441367024FAT4c.1281C>T (p.Asp427=)
c.-55+1715C>T (n.-55+1715C>T)
4g.125317693C>ACA358117581FAT4c.1282C>A (p.Arg428Ser)
c.-55+1716C>A (n.-55+1716C>A)
dbSNP gnomAD v2 gnomAD v4
4g.125317693C=CA1491600487FAT4c.1282C= (p.Arg428=)
c.-55+1716C= (n.-55+1716C=)
4g.125317693C>GCA358117582FAT4c.1282C>G (p.Arg428Gly)
c.-55+1716C>G (n.-55+1716C>G)
4g.125317693C>TCA358117583FAT4c.1282C>T (p.Arg428Cys)
c.-55+1716C>T (n.-55+1716C>T)
gnomAD v4
4g.125317694G>ACA358117584FAT4c.1283G>A (p.Arg428His)
c.-55+1717G>A (n.-55+1717G>A)
dbSNP
4g.125317694G>CCA358117585FAT4c.1283G>C (p.Arg428Pro)
c.-55+1717G>C (n.-55+1717G>C)
4g.125317694G>TCA358117586FAT4c.1283G>T (p.Arg428Leu)
c.-55+1717G>T (n.-55+1717G>T)
4g.125317695C>ACA441367034FAT4c.1284C>A (p.Arg428=)
c.-55+1718C>A (n.-55+1718C>A)
4g.125317695C=CA1491600490FAT4c.1284C= (p.Arg428=)
c.-55+1718C= (n.-55+1718C=)
4g.125317695C>GCA441367035FAT4c.1284C>G (p.Arg428=)
c.-55+1718C>G (n.-55+1718C>G)
gnomAD v4
4g.125317695C>TCA104862152FAT4c.1284C>T (p.Arg428=)
c.-55+1718C>T (n.-55+1718C>T)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.125317696G>ACA358117589FAT4c.1285G>A (p.Glu429Lys)
c.-55+1719G>A (n.-55+1719G>A)
4g.125317696G>CCA358117587FAT4c.1285G>C (p.Glu429Gln)
c.-55+1719G>C (n.-55+1719G>C)
gnomAD v4
4g.125317696G>TCA358117588FAT4c.1285G>T (p.Glu429Ter)
c.-55+1719G>T (n.-55+1719G>T)
4g.125317697A>CCA358117590FAT4c.1286A>C (p.Glu429Ala)
c.-55+1720A>C (n.-55+1720A>C)
4g.125317697A>GCA358117591FAT4c.1286A>G (p.Glu429Gly)
c.-55+1720A>G (n.-55+1720A>G)
4g.125317697A>TCA358117592FAT4c.1286A>T (p.Glu429Val)
c.-55+1720A>T (n.-55+1720A>T)
4g.125317698G>ACA441367046FAT4c.1287G>A (p.Glu429=)
c.-55+1721G>A (n.-55+1721G>A)
dbSNP gnomAD v2 gnomAD v4
4g.125317698G>CCA358117593FAT4c.1287G>C (p.Glu429Asp)
c.-55+1721G>C (n.-55+1721G>C)
4g.125317698G=CA1491600495FAT4c.1287G= (p.Glu429=)
c.-55+1721G= (n.-55+1721G=)
4g.125317698G>TCA358117594FAT4c.1287G>T (p.Glu429Asp)
c.-55+1721G>T (n.-55+1721G>T)
4g.125317699C>ACA358117595FAT4c.1288C>A (p.Arg430Ser)
c.-55+1722C>A (n.-55+1722C>A)
4g.125317699C>GCA358117596FAT4c.1288C>G (p.Arg430Gly)
c.-55+1722C>G (n.-55+1722C>G)
gnomAD v4
4g.125317699C>TCA358117597FAT4c.1288C>T (p.Arg430Cys)
c.-55+1722C>T (n.-55+1722C>T)
4g.125317700G>ACA3071955FAT4c.1289G>A (p.Arg430His)
c.-55+1723G>A (n.-55+1723G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.125317700G>CCA358117598FAT4c.1289G>C (p.Arg430Pro)
c.-55+1723G>C (n.-55+1723G>C)
dbSNP gnomAD v4
4g.125317700G=CA1491600500FAT4c.1289G= (p.Arg430=)
c.-55+1723G= (n.-55+1723G=)
4g.125317700G>TCA3071956FAT4c.1289G>T (p.Arg430Leu)
c.-55+1723G>T (n.-55+1723G>T)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched