Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.31536285G>ACA042701DSG2c.1507G>A (p.Val503Met)
c.973G>A (p.Val325Met)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536285G>CCA402141523DSG2c.1507G>C (p.Val503Leu)
c.973G>C (p.Val325Leu)
18g.31536285G=CA2293861955DSG2c.1507G= (p.Val503=)
c.973G= (p.Val325=)
18g.31536285G>TCA402141525DSG2c.1507G>T (p.Val503Leu)
c.973G>T (p.Val325Leu)
18g.31536286T>ACA402141531DSG2c.1508T>A (p.Val503Glu)
c.974T>A (p.Val325Glu)
18g.31536286T>CCA402141533DSG2c.1508T>C (p.Val503Ala)
c.974T>C (p.Val325Ala)
 gnomAD v4
18g.31536286T>GCA042711DSG2c.1508T>G (p.Val503Gly)
c.974T>G (p.Val325Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536286T=CA2293861956DSG2c.1508T= (p.Val503=)
c.974T= (p.Val325=)
18g.31536287G>ACA503600713DSG2c.1509G>A (p.Val503=)
c.975G>A (p.Val325=)
 dbSNP
18g.31536287G>CCA503600715DSG2c.1509G>C (p.Val503=)
c.975G>C (p.Val325=)
18g.31536287G=CA2293861957DSG2c.1509G= (p.Val503=)
c.975G= (p.Val325=)
18g.31536287G>TCA503600714DSG2c.1509G>T (p.Val503=)
c.975G>T (p.Val325=)
18g.31536288C>ACA402141535DSG2c.1510C>A (p.Gln504Lys)
c.976C>A (p.Gln326Lys)
18g.31536288C>GCA402141538DSG2c.1510C>G (p.Gln504Glu)
c.976C>G (p.Gln326Glu)
18g.31536288C>TCA402141540DSG2c.1510C>T (p.Gln504Ter)
c.976C>T (p.Gln326Ter)
18g.31536289A=CA2293861958DSG2c.1511A= (p.Gln504=)
c.977A= (p.Gln326=)
18g.31536289A>CCA402141542DSG2c.1511A>C (p.Gln504Pro)
c.977A>C (p.Gln326Pro)
 dbSNP gnomAD v4
18g.31536289A>GCA402141545DSG2c.1511A>G (p.Gln504Arg)
c.977A>G (p.Gln326Arg)
18g.31536289A>TCA402141548DSG2c.1511A>T (p.Gln504Leu)
c.977A>T (p.Gln326Leu)
18g.31536290G>ACA503600716DSG2c.1512G>A (p.Gln504=)
c.978G>A (p.Gln326=)
18g.31536290G>CCA402141551DSG2c.1512G>C (p.Gln504His)
c.978G>C (p.Gln326His)
18g.31536290G>TCA402141549DSG2c.1512G>T (p.Gln504His)
c.978G>T (p.Gln326His)
18g.31536291A>CCA402141553DSG2c.1513A>C (p.Thr505Pro)
c.979A>C (p.Thr327Pro)
18g.31536291A>GCA402141555DSG2c.1513A>G (p.Thr505Ala)
c.979A>G (p.Thr327Ala)
 ClinVar
18g.31536291A>TCA402141557DSG2c.1513A>T (p.Thr505Ser)
c.979A>T (p.Thr327Ser)
18g.31536292C>ACA402141559DSG2c.1514C>A (p.Thr505Lys)
c.980C>A (p.Thr327Lys)
18g.31536292C>GCA402141561DSG2c.1514C>G (p.Thr505Arg)
c.980C>G (p.Thr327Arg)
18g.31536292C>TCA402141564DSG2c.1514C>T (p.Thr505Ile)
c.980C>T (p.Thr327Ile)
 COSMIC
18g.31536293A=CA2293861959DSG2c.1515A= (p.Thr505=)
c.981A= (p.Thr327=)
18g.31536293A>CCA503600717DSG2c.1515A>C (p.Thr505=)
c.981A>C (p.Thr327=)
 ClinVar
18g.31536293A>GCA503600718DSG2c.1515A>G (p.Thr505=)
c.981A>G (p.Thr327=)
18g.31536293A>TCA503600719DSG2c.1515A>T (p.Thr505=)
c.981A>T (p.Thr327=)
 ClinVar dbSNP
18g.31536294A>CCA402141565DSG2c.1516A>C (p.Ile506Leu)
c.982A>C (p.Ile328Leu)
18g.31536294A>GCA402141568DSG2c.1516A>G (p.Ile506Val)
c.982A>G (p.Ile328Val)
18g.31536294A>TCA402141570DSG2c.1516A>T (p.Ile506Phe)
c.982A>T (p.Ile328Phe)
18g.31536295T>ACA402141572DSG2c.1517T>A (p.Ile506Asn)
c.983T>A (p.Ile328Asn)
18g.31536295T>CCA402141575DSG2c.1517T>C (p.Ile506Thr)
c.983T>C (p.Ile328Thr)
18g.31536295T>GCA402141578DSG2c.1517T>G (p.Ile506Ser)
c.983T>G (p.Ile328Ser)
18g.31536296C>ACA503600721DSG2c.1518C>A (p.Ile506=)
c.984C>A (p.Ile328=)
18g.31536296C>GCA402141581DSG2c.1518C>G (p.Ile506Met)
c.984C>G (p.Ile328Met)
 gnomAD v4
18g.31536296C>TCA503600720DSG2c.1518C>T (p.Ile506=)
c.984C>T (p.Ile328=)
18g.31536297T>ACA402141596DSG2c.1519T>A (p.Cys507Ser)
c.985T>A (p.Cys329Ser)
18g.31536297T>CCA402141584DSG2c.1519T>C (p.Cys507Arg)
c.985T>C (p.Cys329Arg)
18g.31536297T>GCA402141586DSG2c.1519T>G (p.Cys507Gly)
c.985T>G (p.Cys329Gly)
18g.31536298G>ACA021434DSG2c.1520G>A (p.Cys507Tyr)
c.986G>A (p.Cys329Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31536298G>CCA402141601DSG2c.1520G>C (p.Cys507Ser)
c.986G>C (p.Cys329Ser)
 ClinVar dbSNP
18g.31536298G=CA2293861960DSG2c.1520G= (p.Cys507=)
c.986G= (p.Cys329=)
18g.31536298G>TCA042740DSG2c.1520G>T (p.Cys507Phe)
c.986G>T (p.Cys329Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536299T>ACA402141605DSG2c.1521T>A (p.Cys507Ter)
c.987T>A (p.Cys329Ter)
18g.31536299T>CCA503600722DSG2c.1521T>C (p.Cys507=)
c.987T>C (p.Cys329=)
18g.31536299T>GCA402141606DSG2c.1521T>G (p.Cys507Trp)
c.987T>G (p.Cys329Trp)
 gnomAD v4
18g.31536300C>ACA402141609DSG2c.1522C>A (p.His508Asn)
c.988C>A (p.His330Asn)
18g.31536300C>GCA402141615DSG2c.1522C>G (p.His508Asp)
c.988C>G (p.His330Asp)
18g.31536300C>TCA402141616DSG2c.1522C>T (p.His508Tyr)
c.988C>T (p.His330Tyr)
18g.31536301A=CA2293861961DSG2c.1523A= (p.His508=)
c.989A= (p.His330=)
18g.31536301A>CCA402141618DSG2c.1523A>C (p.His508Pro)
c.989A>C (p.His330Pro)
18g.31536301A>GCA402141620DSG2c.1523A>G (p.His508Arg)
c.989A>G (p.His330Arg)
18g.31536301A>TCA042751DSG2c.1523A>T (p.His508Leu)
c.989A>T (p.His330Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536302C>ACA402141627DSG2c.1524C>A (p.His508Gln)
c.990C>A (p.His330Gln)
 ClinVar dbSNP
18g.31536302C=CA2293861962DSG2c.1524C= (p.His508=)
c.990C= (p.His330=)
18g.31536302C>GCA402141624DSG2c.1524C>G (p.His508Gln)
c.990C>G (p.His330Gln)
18g.31536302C>TCA042763DSG2c.1524C>T (p.His508=)
c.990C>T (p.His330=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536303G>ACA042777DSG2c.1525G>A (p.Asp509Asn)
c.991G>A (p.Asp331Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.31536303G>CCA402141631DSG2c.1525G>C (p.Asp509His)
c.991G>C (p.Asp331His)
18g.31536303G=CA2293861963DSG2c.1525G= (p.Asp509=)
c.991G= (p.Asp331=)
18g.31536303G>TCA402141634DSG2c.1525G>T (p.Asp509Tyr)
c.991G>T (p.Asp331Tyr)
18g.31536304A>CCA402141636DSG2c.1526A>C (p.Asp509Ala)
c.992A>C (p.Asp331Ala)
18g.31536304A>GCA402141637DSG2c.1526A>G (p.Asp509Gly)
c.992A>G (p.Asp331Gly)
18g.31536304A>TCA402141639DSG2c.1526A>T (p.Asp509Val)
c.992A>T (p.Asp331Val)
18g.31536305T>ACA297741511DSG2c.1527T>A (p.Asp509Glu)
c.993T>A (p.Asp331Glu)
 ClinVar dbSNP
18g.31536305T>CCA503600723DSG2c.1527T>C (p.Asp509=)
c.993T>C (p.Asp331=)
18g.31536305T>GCA402141647DSG2c.1527T>G (p.Asp509Glu)
c.993T>G (p.Asp331Glu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31536305T=CA2293861964DSG2c.1527T= (p.Asp509=)
c.993T= (p.Asp331=)
18g.31536306G>ACA402141650DSG2c.1528G>A (p.Ala510Thr)
c.994G>A (p.Ala332Thr)
 ClinVar dbSNP gnomAD v4
18g.31536306G>CCA402141652DSG2c.1528G>C (p.Ala510Pro)
c.994G>C (p.Ala332Pro)
18g.31536306G=CA2293861965DSG2c.1528G= (p.Ala510=)
c.994G= (p.Ala332=)
18g.31536306G>TCA402141654DSG2c.1528G>T (p.Ala510Ser)
c.994G>T (p.Ala332Ser)
18g.31536306_31536307insTCA2641406715DSG2c.1528_1529insT (p.Ala510ValfsTer26)
c.994_995insT (p.Ala332ValfsTer26)
 gnomAD v4
18g.31536307C>ACA402141660DSG2c.1529C>A (p.Ala510Glu)
c.995C>A (p.Ala332Glu)
 gnomAD v4
18g.31536307C>GCA402141659DSG2c.1529C>G (p.Ala510Gly)
c.995C>G (p.Ala332Gly)
18g.31536307C>TCA402141658DSG2c.1529C>T (p.Ala510Val)
c.995C>T (p.Ala332Val)
 gnomAD v4
18g.31536308A>CCA503600724DSG2c.1530A>C (p.Ala510=)
c.996A>C (p.Ala332=)
18g.31536308A>GCA503600725DSG2c.1530A>G (p.Ala510=)
c.996A>G (p.Ala332=)
18g.31536308A>TCA503600726DSG2c.1530A>T (p.Ala510=)
c.996A>T (p.Ala332=)
18g.31536310_31536311delCA2641406716DSG2c.1532_1533del (p.Glu511ValfsTer24)
c.998_999del (p.Glu333ValfsTer24)
 gnomAD v4
18g.31536309G>ACA402141661DSG2c.1531G>A (p.Glu511Lys)
c.997G>A (p.Glu333Lys)
18g.31536309G>CCA402141665DSG2c.1531G>C (p.Glu511Gln)
c.997G>C (p.Glu333Gln)
 dbSNP
18g.31536309G>TCA402141663DSG2c.1531G>T (p.Glu511Ter)
c.997G>T (p.Glu333Ter)
18g.31536310A=CA2293861966DSG2c.1532A= (p.Glu511=)
c.998A= (p.Glu333=)
18g.31536310A>CCA402141667DSG2c.1532A>C (p.Glu511Ala)
c.998A>C (p.Glu333Ala)
18g.31536310A>GCA402141669DSG2c.1532A>G (p.Glu511Gly)
c.998A>G (p.Glu333Gly)
 ClinVar dbSNP gnomAD v2
18g.31536310A>TCA402141671DSG2c.1532A>T (p.Glu511Val)
c.998A>T (p.Glu333Val)
 gnomAD v4
18g.31536311G>ACA042791DSG2c.1533G>A (p.Glu511=)
c.999G>A (p.Glu333=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536311G>CCA402141674DSG2c.1533G>C (p.Glu511Asp)
c.999G>C (p.Glu333Asp)
 ClinVar dbSNP
18g.31536311G=CA2293861967DSG2c.1533G= (p.Glu511=)
c.999G= (p.Glu333=)
18g.31536311G>TCA402141676DSG2c.1533G>T (p.Glu511Asp)
c.999G>T (p.Glu333Asp)
18g.31536312T>ACA402141679DSG2c.1534T>A (p.Tyr512Asn)
c.1000T>A (p.Tyr334Asn)
18g.31536312T>CCA402141682DSG2c.1534T>C (p.Tyr512His)
c.1000T>C (p.Tyr334His)
18g.31536312T>GCA402141684DSG2c.1534T>G (p.Tyr512Asp)
c.1000T>G (p.Tyr334Asp)
18g.31536313A>CCA402141685DSG2c.1535A>C (p.Tyr512Ser)
c.1001A>C (p.Tyr334Ser)
18g.31536313A>GCA402141688DSG2c.1535A>G (p.Tyr512Cys)
c.1001A>G (p.Tyr334Cys)
18g.31536313A>TCA402141690DSG2c.1535A>T (p.Tyr512Phe)
c.1001A>T (p.Tyr334Phe)
18g.31536314T>ACA402141695DSG2c.1536T>A (p.Tyr512Ter)
c.1002T>A (p.Tyr334Ter)
18g.31536314T>CCA297741517DSG2c.1536T>C (p.Tyr512=)
c.1002T>C (p.Tyr334=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31536314T>GCA402141693DSG2c.1536T>G (p.Tyr512Ter)
c.1002T>G (p.Tyr334Ter)
18g.31536314T=CA2293861968DSG2c.1536T= (p.Tyr512=)
c.1002T= (p.Tyr334=)
18g.31536315G>ACA402141697DSG2c.1537G>A (p.Val513Met)
c.1003G>A (p.Val335Met)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.31536315G>CCA402141702DSG2c.1537G>C (p.Val513Leu)
c.1003G>C (p.Val335Leu)
18g.31536315G=CA2293861969DSG2c.1537G= (p.Val513=)
c.1003G= (p.Val335=)
18g.31536315G>TCA402141704DSG2c.1537G>T (p.Val513Leu)
c.1003G>T (p.Val335Leu)
 ClinVar dbSNP
18g.31536316T>ACA402141707DSG2c.1538T>A (p.Val513Glu)
c.1004T>A (p.Val335Glu)
18g.31536316T>CCA402141709DSG2c.1538T>C (p.Val513Ala)
c.1004T>C (p.Val335Ala)
 gnomAD v4
18g.31536316T>GCA402141711DSG2c.1538T>G (p.Val513Gly)
c.1004T>G (p.Val335Gly)
18g.31536317G>ACA503600727DSG2c.1539G>A (p.Val513=)
c.1005G>A (p.Val335=)
18g.31536317G>CCA503600729DSG2c.1539G>C (p.Val513=)
c.1005G>C (p.Val335=)
 ClinVar dbSNP
18g.31536317G>TCA503600728DSG2c.1539G>T (p.Val513=)
c.1005G>T (p.Val335=)
18g.31536318A=CA2293861970DSG2c.1540A= (p.Asn514=)
c.1006A= (p.Asn336=)
18g.31536318A>CCA402141713DSG2c.1540A>C (p.Asn514His)
c.1006A>C (p.Asn336His)
18g.31536318A>GCA402141716DSG2c.1540A>G (p.Asn514Asp)
c.1006A>G (p.Asn336Asp)
 ClinVar dbSNP
18g.31536318A>TCA402141717DSG2c.1540A>T (p.Asn514Tyr)
c.1006A>T (p.Asn336Tyr)
18g.31536319A=CA2293861971DSG2c.1541A= (p.Asn514=)
c.1007A= (p.Asn336=)
18g.31536319A>CCA297741523DSG2c.1541A>C (p.Asn514Thr)
c.1007A>C (p.Asn336Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
18g.31536319A>GCA402141721DSG2c.1541A>G (p.Asn514Ser)
c.1007A>G (p.Asn336Ser)
 gnomAD v4
18g.31536319A>TCA402141724DSG2c.1541A>T (p.Asn514Ile)
c.1007A>T (p.Asn336Ile)
 ClinVar dbSNP gnomAD v4
18g.31536320T>ACA402141729DSG2c.1542T>A (p.Asn514Lys)
c.1008T>A (p.Asn336Lys)
18g.31536320T>CCA503600730DSG2c.1542T>C (p.Asn514=)
c.1008T>C (p.Asn336=)
18g.31536320T>GCA402141727DSG2c.1542T>G (p.Asn514Lys)
c.1008T>G (p.Asn336Lys)
18g.31536321G>ACA021458DSG2c.1543G>A (p.Val515Ile)
c.1009G>A (p.Val337Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536321G>CCA402141733DSG2c.1543G>C (p.Val515Leu)
c.1009G>C (p.Val337Leu)
18g.31536321G=CA2293861972DSG2c.1543G= (p.Val515=)
c.1009G= (p.Val337=)
18g.31536321G>TCA042820DSG2c.1543G>T (p.Val515Phe)
c.1009G>T (p.Val337Phe)
 ClinVar dbSNP ExAC gnomAD v2 COSMIC
18g.31536322T>ACA402141735DSG2c.1544T>A (p.Val515Asp)
c.1010T>A (p.Val337Asp)
18g.31536322T>CCA402141737DSG2c.1544T>C (p.Val515Ala)
c.1010T>C (p.Val337Ala)
 gnomAD v4
18g.31536322T>GCA402141738DSG2c.1544T>G (p.Val515Gly)
c.1010T>G (p.Val337Gly)
18g.31536323T>ACA503600731DSG2c.1545T>A (p.Val515=)
c.1011T>A (p.Val337=)
18g.31536323T>CCA503600732DSG2c.1545T>C (p.Val515=)
c.1011T>C (p.Val337=)
 COSMIC
18g.31536323T>GCA503600733DSG2c.1545T>G (p.Val515=)
c.1011T>G (p.Val337=)
18g.31536324A>CCA402141745DSG2c.1546A>C (p.Thr516Pro)
c.1012A>C (p.Thr338Pro)
18g.31536324A>GCA402141742DSG2c.1546A>G (p.Thr516Ala)
c.1012A>G (p.Thr338Ala)
 ClinVar gnomAD v4
18g.31536324A>TCA402141740DSG2c.1546A>T (p.Thr516Ser)
c.1012A>T (p.Thr338Ser)
18g.31536325C>ACA402141746DSG2c.1547C>A (p.Thr516Asn)
c.1013C>A (p.Thr338Asn)
18g.31536325C>GCA402141749DSG2c.1547C>G (p.Thr516Ser)
c.1013C>G (p.Thr338Ser)
18g.31536325C>TCA402141750DSG2c.1547C>T (p.Thr516Ile)
c.1013C>T (p.Thr338Ile)
18g.31536326T>ACA503600734DSG2c.1548T>A (p.Thr516=)
c.1014T>A (p.Thr338=)
18g.31536326T>CCA503600735DSG2c.1548T>C (p.Thr516=)
c.1014T>C (p.Thr338=)
 ClinVar dbSNP gnomAD v4
18g.31536326T>GCA503600736DSG2c.1548T>G (p.Thr516=)
c.1014T>G (p.Thr338=)
18g.31536326T=CA2293861973DSG2c.1548T= (p.Thr516=)
c.1014T= (p.Thr338=)
18g.31536327G>ACA402141753DSG2c.1549G>A (p.Ala517Thr)
c.1015G>A (p.Ala339Thr)
 ClinVar
18g.31536327G>CCA402141754DSG2c.1549G>C (p.Ala517Pro)
c.1015G>C (p.Ala339Pro)
18g.31536327G=CA2293861974DSG2c.1549G= (p.Ala517=)
c.1015G= (p.Ala339=)
18g.31536327G>TCA402141755DSG2c.1549G>T (p.Ala517Ser)
c.1015G>T (p.Ala339Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.31536328C>ACA402141758DSG2c.1550C>A (p.Ala517Glu)
c.1016C>A (p.Ala339Glu)
 gnomAD v4
18g.31536328C=CA2293861975DSG2c.1550C= (p.Ala517=)
c.1016C= (p.Ala339=)
18g.31536328C>GCA402141761DSG2c.1550C>G (p.Ala517Gly)
c.1016C>G (p.Ala339Gly)
18g.31536328C>TCA021465DSG2c.1550C>T (p.Ala517Val)
c.1016C>T (p.Ala339Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536329A>CCA503600737DSG2c.1551A>C (p.Ala517=)
c.1017A>C (p.Ala339=)
18g.31536329A>GCA503600739DSG2c.1551A>G (p.Ala517=)
c.1017A>G (p.Ala339=)
18g.31536329A>TCA503600738DSG2c.1551A>T (p.Ala517=)
c.1017A>T (p.Ala339=)
18g.31536330G>ACA402141764DSG2c.1552G>A (p.Glu518Lys)
c.1018G>A (p.Glu340Lys)
18g.31536330G>CCA402141765DSG2c.1552G>C (p.Glu518Gln)
c.1018G>C (p.Glu340Gln)
 COSMIC
18g.31536330G>TCA402141767DSG2c.1552G>T (p.Glu518Ter)
c.1018G>T (p.Glu340Ter)
18g.31536331A>CCA402141770DSG2c.1553A>C (p.Glu518Ala)
c.1019A>C (p.Glu340Ala)
18g.31536331A>GCA402141773DSG2c.1553A>G (p.Glu518Gly)
c.1019A>G (p.Glu340Gly)
 ClinVar dbSNP
18g.31536331A>TCA402141774DSG2c.1553A>T (p.Glu518Val)
c.1019A>T (p.Glu340Val)
18g.31536332G>ACA503600740DSG2c.1554G>A (p.Glu518=)
c.1020G>A (p.Glu340=)
 ClinVar dbSNP gnomAD v4
18g.31536332G>CCA402141776DSG2c.1554G>C (p.Glu518Asp)
c.1020G>C (p.Glu340Asp)
18g.31536332G>TCA402141777DSG2c.1554G>T (p.Glu518Asp)
c.1020G>T (p.Glu340Asp)
18g.31536333G>ACA402141780DSG2c.1555G>A (p.Asp519Asn)
c.1021G>A (p.Asp341Asn)
 dbSNP gnomAD v3 gnomAD v4
18g.31536333G>CCA402141782DSG2c.1555G>C (p.Asp519His)
c.1021G>C (p.Asp341His)
 ClinVar dbSNP gnomAD v4
18g.31536333G=CA2293861976DSG2c.1555G= (p.Asp519=)
c.1021G= (p.Asp341=)
18g.31536333G>TCA021474DSG2c.1555G>T (p.Asp519Tyr)
c.1021G>T (p.Asp341Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536334A>CCA402141785DSG2c.1556A>C (p.Asp519Ala)
c.1022A>C (p.Asp341Ala)
18g.31536334A>GCA402141787DSG2c.1556A>G (p.Asp519Gly)
c.1022A>G (p.Asp341Gly)
 COSMIC
18g.31536334A>TCA402141786DSG2c.1556A>T (p.Asp519Val)
c.1022A>T (p.Asp341Val)
18g.31536335C>ACA402141789DSG2c.1557C>A (p.Asp519Glu)
c.1023C>A (p.Asp341Glu)
 dbSNP gnomAD v4
18g.31536335C=CA2293861977DSG2c.1557C= (p.Asp519=)
c.1023C= (p.Asp341=)
18g.31536335C>GCA402141790DSG2c.1557C>G (p.Asp519Glu)
c.1023C>G (p.Asp341Glu)
18g.31536335C>TCA503600741DSG2c.1557C>T (p.Asp519=)
c.1023C>T (p.Asp341=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
18g.31536336C>ACA402141793DSG2c.1558C>A (p.Leu520Met)
c.1024C>A (p.Leu342Met)
18g.31536336C>GCA402141794DSG2c.1558C>G (p.Leu520Val)
c.1024C>G (p.Leu342Val)
18g.31536336C>TCA503600742DSG2c.1558C>T (p.Leu520=)
c.1024C>T (p.Leu342=)
18g.31536337T>ACA402141796DSG2c.1559T>A (p.Leu520Gln)
c.1025T>A (p.Leu342Gln)
18g.31536337T>CCA402141798DSG2c.1559T>C (p.Leu520Pro)
c.1025T>C (p.Leu342Pro)
18g.31536337T>GCA402141799DSG2c.1559T>G (p.Leu520Arg)
c.1025T>G (p.Leu342Arg)
18g.31536338G>ACA503600743DSG2c.1560G>A (p.Leu520=)
c.1026G>A (p.Leu342=)
18g.31536338G>CCA503600744DSG2c.1560G>C (p.Leu520=)
c.1026G>C (p.Leu342=)
18g.31536338G>TCA503600745DSG2c.1560G>T (p.Leu520=)
c.1026G>T (p.Leu342=)
18g.31536339G>ACA402141802DSG2c.1561G>A (p.Asp521Asn)
c.1027G>A (p.Asp343Asn)
 ClinVar dbSNP gnomAD v4
18g.31536339G>CCA402141803DSG2c.1561G>C (p.Asp521His)
c.1027G>C (p.Asp343His)
18g.31536339G>TCA402141806DSG2c.1561G>T (p.Asp521Tyr)
c.1027G>T (p.Asp343Tyr)
 COSMIC
18g.31536340A=CA2293861978DSG2c.1562A= (p.Asp521=)
c.1028A= (p.Asp343=)
18g.31536340A>CCA402141812DSG2c.1562A>C (p.Asp521Ala)
c.1028A>C (p.Asp343Ala)
18g.31536340A>GCA021483DSG2c.1562A>G (p.Asp521Gly)
c.1028A>G (p.Asp343Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536340A>TCA402141810DSG2c.1562A>T (p.Asp521Val)
c.1028A>T (p.Asp343Val)
 ClinVar dbSNP gnomAD v4
18g.31536341T>ACA402141815DSG2c.1563T>A (p.Asp521Glu)
c.1029T>A (p.Asp343Glu)
18g.31536341T>CCA503600746DSG2c.1563T>C (p.Asp521=)
c.1029T>C (p.Asp343=)
18g.31536341T>GCA402141816DSG2c.1563T>G (p.Asp521Glu)
c.1029T>G (p.Asp343Glu)
18g.31536342G>ACA402141818DSG2c.1564G>A (p.Gly522Arg)
c.1030G>A (p.Gly344Arg)
18g.31536342G>CCA402141819DSG2c.1564G>C (p.Gly522Arg)
c.1030G>C (p.Gly344Arg)
18g.31536342G>TCA402141820DSG2c.1564G>T (p.Gly522Ter)
c.1030G>T (p.Gly344Ter)
18g.31536343G>ACA402141822DSG2c.1565G>A (p.Gly522Glu)
c.1031G>A (p.Gly344Glu)
18g.31536343G>CCA402141826DSG2c.1565G>C (p.Gly522Ala)
c.1031G>C (p.Gly344Ala)
18g.31536343G>TCA402141824DSG2c.1565G>T (p.Gly522Val)
c.1031G>T (p.Gly344Val)
18g.31536344A>CCA503600749DSG2c.1566A>C (p.Gly522=)
c.1032A>C (p.Gly344=)
18g.31536344A>GCA503600747DSG2c.1566A>G (p.Gly522=)
c.1032A>G (p.Gly344=)
18g.31536344A>TCA503600748DSG2c.1566A>T (p.Gly522=)
c.1032A>T (p.Gly344=)
18g.31536345C>ACA402141829DSG2c.1567C>A (p.His523Asn)
c.1033C>A (p.His345Asn)
18g.31536345C>GCA402141831DSG2c.1567C>G (p.His523Asp)
c.1033C>G (p.His345Asp)
18g.31536345C>TCA402141833DSG2c.1567C>T (p.His523Tyr)
c.1033C>T (p.His345Tyr)
 gnomAD v4
18g.31536346delCA2641406717DSG2c.1568del (p.His523ProfsTer24)
c.1034del (p.His345ProfsTer24)
 gnomAD v4
18g.31536346A>CCA402141836DSG2c.1568A>C (p.His523Pro)
c.1034A>C (p.His345Pro)
 gnomAD v4
18g.31536346A>GCA402141838DSG2c.1568A>G (p.His523Arg)
c.1034A>G (p.His345Arg)
18g.31536346A>TCA402141840DSG2c.1568A>T (p.His523Leu)
c.1034A>T (p.His345Leu)
 gnomAD v4
18g.31536347C>ACA402141842DSG2c.1569C>A (p.His523Gln)
c.1035C>A (p.His345Gln)
18g.31536347C>GCA402141844DSG2c.1569C>G (p.His523Gln)
c.1035C>G (p.His345Gln)
 ClinVar gnomAD v4
18g.31536347C>TCA503600750DSG2c.1569C>T (p.His523=)
c.1035C>T (p.His345=)
 gnomAD v4
18g.31536348C>ACA402141846DSG2c.1570C>A (p.Pro524Thr)
c.1036C>A (p.Pro346Thr)
18g.31536348C>GCA402141847DSG2c.1570C>G (p.Pro524Ala)
c.1036C>G (p.Pro346Ala)
18g.31536348C>TCA402141848DSG2c.1570C>T (p.Pro524Ser)
c.1036C>T (p.Pro346Ser)
18g.31536349C>ACA402141852DSG2c.1571C>A (p.Pro524Gln)
c.1037C>A (p.Pro346Gln)
18g.31536349C>GCA402141856DSG2c.1571C>G (p.Pro524Arg)
c.1037C>G (p.Pro346Arg)
18g.31536349C>TCA402141854DSG2c.1571C>T (p.Pro524Leu)
c.1037C>T (p.Pro346Leu)
18g.31536350A>CCA503600751DSG2c.1572A>C (p.Pro524=)
c.1038A>C (p.Pro346=)
18g.31536350A>GCA503600752DSG2c.1572A>G (p.Pro524=)
c.1038A>G (p.Pro346=)
18g.31536350A>TCA503600753DSG2c.1572A>T (p.Pro524=)
c.1038A>T (p.Pro346=)
18g.31536351A=CA2293861979DSG2c.1573A= (p.Asn525=)
c.1039A= (p.Asn347=)
18g.31536351A>CCA402141857DSG2c.1573A>C (p.Asn525His)
c.1039A>C (p.Asn347His)
18g.31536351A>GCA021493DSG2c.1573A>G (p.Asn525Asp)
c.1039A>G (p.Asn347Asp)
 ClinVar dbSNP gnomAD v4
18g.31536351A>TCA402141861DSG2c.1573A>T (p.Asn525Tyr)
c.1039A>T (p.Asn347Tyr)
 dbSNP
18g.31536352A>CCA402141864DSG2c.1574A>C (p.Asn525Thr)
c.1040A>C (p.Asn347Thr)
18g.31536352A>GCA402141866DSG2c.1574A>G (p.Asn525Ser)
c.1040A>G (p.Asn347Ser)
18g.31536352A>TCA402141869DSG2c.1574A>T (p.Asn525Ile)
c.1040A>T (p.Asn347Ile)
18g.31536353C>ACA402141870DSG2c.1575C>A (p.Asn525Lys)
c.1041C>A (p.Asn347Lys)
18g.31536353C=CA2293861980DSG2c.1575C= (p.Asn525=)
c.1041C= (p.Asn347=)
18g.31536353C>GCA402141871DSG2c.1575C>G (p.Asn525Lys)
c.1041C>G (p.Asn347Lys)
 dbSNP
18g.31536353C>TCA503600754DSG2c.1575C>T (p.Asn525=)
c.1041C>T (p.Asn347=)
 gnomAD v4
18g.31536354A>CCA402141872DSG2c.1576A>C (p.Ser526Arg)
c.1042A>C (p.Ser348Arg)
18g.31536354A>GCA402141873DSG2c.1576A>G (p.Ser526Gly)
c.1042A>G (p.Ser348Gly)
 gnomAD v4
18g.31536354A>TCA402141874DSG2c.1576A>T (p.Ser526Cys)
c.1042A>T (p.Ser348Cys)
18g.31536355G>ACA402141877DSG2c.1577G>A (p.Ser526Asn)
c.1043G>A (p.Ser348Asn)
 ClinVar dbSNP gnomAD v4
18g.31536355G>CCA042877DSG2c.1577G>C (p.Ser526Thr)
c.1043G>C (p.Ser348Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536355G=CA2293861981DSG2c.1577G= (p.Ser526=)
c.1043G= (p.Ser348=)
18g.31536355G>TCA402141875DSG2c.1577G>T (p.Ser526Ile)
c.1043G>T (p.Ser348Ile)
18g.31536356T>ACA402141879DSG2c.1578T>A (p.Ser526Arg)
c.1044T>A (p.Ser348Arg)
18g.31536356T>CCA042892DSG2c.1578T>C (p.Ser526=)
c.1044T>C (p.Ser348=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536356T>GCA402141881DSG2c.1578T>G (p.Ser526Arg)
c.1044T>G (p.Ser348Arg)
18g.31536356T=CA2293861982DSG2c.1578T= (p.Ser526=)
c.1044T= (p.Ser348=)
18g.31536357G>ACA402141884DSG2c.1579G>A (p.Gly527Ser)
c.1045G>A (p.Gly349Ser)
 dbSNP gnomAD v3 gnomAD v4
18g.31536357G>CCA402141885DSG2c.1579G>C (p.Gly527Arg)
c.1045G>C (p.Gly349Arg)
18g.31536357G=CA2293861983DSG2c.1579G= (p.Gly527=)
c.1045G= (p.Gly349=)
18g.31536357G>TCA402141888DSG2c.1579G>T (p.Gly527Cys)
c.1045G>T (p.Gly349Cys)
18g.31536358G>ACA402141889DSG2c.1580G>A (p.Gly527Asp)
c.1046G>A (p.Gly349Asp)
 gnomAD v4
18g.31536358G>CCA402141890DSG2c.1580G>C (p.Gly527Ala)
c.1046G>C (p.Gly349Ala)
18g.31536358G>TCA402141892DSG2c.1580G>T (p.Gly527Val)
c.1046G>T (p.Gly349Val)
18g.31536359C>ACA503600755DSG2c.1581C>A (p.Gly527=)
c.1047C>A (p.Gly349=)
18g.31536359C>GCA503600756DSG2c.1581C>G (p.Gly527=)
c.1047C>G (p.Gly349=)
18g.31536359C>TCA503600757DSG2c.1581C>T (p.Gly527=)
c.1047C>T (p.Gly349=)
18g.31536360C>ACA402141894DSG2c.1582C>A (p.Pro528Thr)
c.1048C>A (p.Pro350Thr)
18g.31536360C=CA2293861984DSG2c.1582C= (p.Pro528=)
c.1048C= (p.Pro350=)
18g.31536360C>GCA042913DSG2c.1582C>G (p.Pro528Ala)
c.1048C>G (p.Pro350Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.31536360C>TCA402141896DSG2c.1582C>T (p.Pro528Ser)
c.1048C>T (p.Pro350Ser)
18g.31536361C>ACA402141900DSG2c.1583C>A (p.Pro528His)
c.1049C>A (p.Pro350His)
18g.31536361C=CA2293861985DSG2c.1583C= (p.Pro528=)
c.1049C= (p.Pro350=)
18g.31536361C>GCA402141902DSG2c.1583C>G (p.Pro528Arg)
c.1049C>G (p.Pro350Arg)
 ClinVar dbSNP gnomAD v4
18g.31536361C>TCA297741569DSG2c.1583C>T (p.Pro528Leu)
c.1049C>T (p.Pro350Leu)
 dbSNP
18g.31536362T>ACA503600758DSG2c.1584T>A (p.Pro528=)
c.1050T>A (p.Pro350=)
18g.31536362T>CCA503600759DSG2c.1584T>C (p.Pro528=)
c.1050T>C (p.Pro350=)
18g.31536362T>GCA503600760DSG2c.1584T>G (p.Pro528=)
c.1050T>G (p.Pro350=)
18g.31536363T>ACA402141910DSG2c.1585T>A (p.Phe529Ile)
c.1051T>A (p.Phe351Ile)
18g.31536363T>CCA402141904DSG2c.1585T>C (p.Phe529Leu)
c.1051T>C (p.Phe351Leu)
18g.31536363T>GCA402141906DSG2c.1585T>G (p.Phe529Val)
c.1051T>G (p.Phe351Val)
18g.31536364T>ACA402141913DSG2c.1586T>A (p.Phe529Tyr)
c.1052T>A (p.Phe351Tyr)
18g.31536364T>CCA402141915DSG2c.1586T>C (p.Phe529Ser)
c.1052T>C (p.Phe351Ser)
 dbSNP
18g.31536364T>GCA402141917DSG2c.1586T>G (p.Phe529Cys)
c.1052T>G (p.Phe351Cys)
18g.31536364T=CA2293861986DSG2c.1586T= (p.Phe529=)
c.1052T= (p.Phe351=)
18g.31536365C>ACA402141919DSG2c.1587C>A (p.Phe529Leu)
c.1053C>A (p.Phe351Leu)
18g.31536365C>GCA402141921DSG2c.1587C>G (p.Phe529Leu)
c.1053C>G (p.Phe351Leu)
 gnomAD v4
18g.31536365C>TCA503600761DSG2c.1587C>T (p.Phe529=)
c.1053C>T (p.Phe351=)
18g.31536366A=CA2293861987DSG2c.1588A= (p.Ser530=)
c.1054A= (p.Ser352=)
18g.31536366A>CCA402141924DSG2c.1588A>C (p.Ser530Arg)
c.1054A>C (p.Ser352Arg)
18g.31536366A>GCA402141925DSG2c.1588A>G (p.Ser530Gly)
c.1054A>G (p.Ser352Gly)
 dbSNP gnomAD v2
18g.31536366A>TCA402141926DSG2c.1588A>T (p.Ser530Cys)
c.1054A>T (p.Ser352Cys)
18g.31536367G>ACA402141928DSG2c.1589G>A (p.Ser530Asn)
c.1055G>A (p.Ser352Asn)
18g.31536367G>CCA402141930DSG2c.1589G>C (p.Ser530Thr)
c.1055G>C (p.Ser352Thr)
18g.31536367G>TCA402141932DSG2c.1589G>T (p.Ser530Ile)
c.1055G>T (p.Ser352Ile)
18g.31536368T>ACA402141935DSG2c.1590T>A (p.Ser530Arg)
c.1056T>A (p.Ser352Arg)
18g.31536368T>CCA503600762DSG2c.1590T>C (p.Ser530=)
c.1056T>C (p.Ser352=)
18g.31536368T>GCA402141933DSG2c.1590T>G (p.Ser530Arg)
c.1056T>G (p.Ser352Arg)
18g.31536369T>ACA402141937DSG2c.1591T>A (p.Phe531Ile)
c.1057T>A (p.Phe353Ile)
18g.31536369T>CCA402141939DSG2c.1591T>C (p.Phe531Leu)
c.1057T>C (p.Phe353Leu)
18g.31536369T>GCA402141941DSG2c.1591T>G (p.Phe531Val)
c.1057T>G (p.Phe353Val)
18g.31536370T>ACA402141943DSG2c.1592T>A (p.Phe531Tyr)
c.1058T>A (p.Phe353Tyr)
18g.31536370T>CCA402141945DSG2c.1592T>C (p.Phe531Ser)
c.1058T>C (p.Phe353Ser)
18g.31536370T>GCA021499DSG2c.1592T>G (p.Phe531Cys)
c.1058T>G (p.Phe353Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536370T=CA2293861988DSG2c.1592T= (p.Phe531=)
c.1058T= (p.Phe353=)
18g.31536371C>ACA402141947DSG2c.1593C>A (p.Phe531Leu)
c.1059C>A (p.Phe353Leu)
18g.31536371C>GCA402141948DSG2c.1593C>G (p.Phe531Leu)
c.1059C>G (p.Phe353Leu)
18g.31536371C>TCA503600766DSG2c.1593C>T (p.Phe531=)
c.1059C>T (p.Phe353=)
 ClinVar
18g.31536372T>ACA402141951DSG2c.1594T>A (p.Ser532Thr)
c.1060T>A (p.Ser354Thr)
18g.31536372T>CCA402141953DSG2c.1594T>C (p.Ser532Pro)
c.1060T>C (p.Ser354Pro)
18g.31536372T>GCA402141955DSG2c.1594T>G (p.Ser532Ala)
c.1060T>G (p.Ser354Ala)
18g.31536373C>ACA402141958DSG2c.1595C>A (p.Ser532Tyr)
c.1061C>A (p.Ser354Tyr)
18g.31536373C>GCA402141959DSG2c.1595C>G (p.Ser532Cys)
c.1061C>G (p.Ser354Cys)
 gnomAD v4
18g.31536373C>TCA402141961DSG2c.1595C>T (p.Ser532Phe)
c.1061C>T (p.Ser354Phe)
18g.31536374C>ACA503600768DSG2c.1596C>A (p.Ser532=)
c.1062C>A (p.Ser354=)
18g.31536374C=CA2293861989DSG2c.1596C= (p.Ser532=)
c.1062C= (p.Ser354=)
18g.31536374C>GCA503600769DSG2c.1596C>G (p.Ser532=)
c.1062C>G (p.Ser354=)
18g.31536374C>TCA042931DSG2c.1596C>T (p.Ser532=)
c.1062C>T (p.Ser354=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
18g.31536375G>ACA042947DSG2c.1597G>A (p.Val533Ile)
c.1063G>A (p.Val355Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536375G>CCA402141970DSG2c.1597G>C (p.Val533Leu)
c.1063G>C (p.Val355Leu)
18g.31536375G=CA2293861990DSG2c.1597G= (p.Val533=)
c.1063G= (p.Val355=)
18g.31536375G>TCA402141978DSG2c.1597G>T (p.Val533Phe)
c.1063G>T (p.Val355Phe)
18g.31536376T>ACA402141980DSG2c.1598T>A (p.Val533Asp)
c.1064T>A (p.Val355Asp)
18g.31536376T>CCA402141981DSG2c.1598T>C (p.Val533Ala)
c.1064T>C (p.Val355Ala)
18g.31536376T>GCA402141984DSG2c.1598T>G (p.Val533Gly)
c.1064T>G (p.Val355Gly)
18g.31536377C>ACA503600771DSG2c.1599C>A (p.Val533=)
c.1065C>A (p.Val355=)
18g.31536377C>GCA503600772DSG2c.1599C>G (p.Val533=)
c.1065C>G (p.Val355=)
18g.31536377C>TCA503600774DSG2c.1599C>T (p.Val533=)
c.1065C>T (p.Val355=)
 ClinVar
18g.31536378A>CCA402141987DSG2c.1600A>C (p.Ile534Leu)
c.1066A>C (p.Ile356Leu)
18g.31536378A>GCA402141989DSG2c.1600A>G (p.Ile534Val)
c.1066A>G (p.Ile356Val)
 gnomAD v4
18g.31536378A>TCA402141992DSG2c.1600A>T (p.Ile534Phe)
c.1066A>T (p.Ile356Phe)
18g.31536379T>ACA402141994DSG2c.1601T>A (p.Ile534Asn)
c.1067T>A (p.Ile356Asn)
 gnomAD v4
18g.31536379T>CCA402141996DSG2c.1601T>C (p.Ile534Thr)
c.1067T>C (p.Ile356Thr)
 ClinVar dbSNP
18g.31536379T>GCA402141999DSG2c.1601T>G (p.Ile534Ser)
c.1067T>G (p.Ile356Ser)
18g.31536380T>ACA503600776DSG2c.1602T>A (p.Ile534=)
c.1068T>A (p.Ile356=)
18g.31536380T>CCA503600777DSG2c.1602T>C (p.Ile534=)
c.1068T>C (p.Ile356=)
18g.31536380T>GCA402142004DSG2c.1602T>G (p.Ile534Met)
c.1068T>G (p.Ile356Met)
18g.31536381G>ACA402142008DSG2c.1603G>A (p.Asp535Asn)
c.1069G>A (p.Asp357Asn)
18g.31536381G>CCA402142019DSG2c.1603G>C (p.Asp535His)
c.1069G>C (p.Asp357His)
18g.31536381G>TCA402142007DSG2c.1603G>T (p.Asp535Tyr)
c.1069G>T (p.Asp357Tyr)
18g.31536382A>CCA402142023DSG2c.1604A>C (p.Asp535Ala)
c.1070A>C (p.Asp357Ala)
18g.31536382A>GCA402142032DSG2c.1604A>G (p.Asp535Gly)
c.1070A>G (p.Asp357Gly)
18g.31536382A>TCA402142034DSG2c.1604A>T (p.Asp535Val)
c.1070A>T (p.Asp357Val)
18g.31536383C>ACA042967DSG2c.1605C>A (p.Asp535Glu)
c.1071C>A (p.Asp357Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536383C=CA2293861991DSG2c.1605C= (p.Asp535=)
c.1071C= (p.Asp357=)
18g.31536383C>GCA042988DSG2c.1605C>G (p.Asp535Glu)
c.1071C>G (p.Asp357Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31536383C>TCA503600778DSG2c.1605C>T (p.Asp535=)
c.1071C>T (p.Asp357=)
18g.31536384A>CCA402142044DSG2c.1606A>C (p.Lys536Gln)
c.1072A>C (p.Lys358Gln)
18g.31536384A>GCA402142038DSG2c.1606A>G (p.Lys536Glu)
c.1072A>G (p.Lys358Glu)
18g.31536384A>TCA402142042DSG2c.1606A>T (p.Lys536Ter)
c.1072A>T (p.Lys358Ter)
18g.31536385A>CCA402142046DSG2c.1607A>C (p.Lys536Thr)
c.1073A>C (p.Lys358Thr)
18g.31536385A>GCA402142047DSG2c.1607A>G (p.Lys536Arg)
c.1073A>G (p.Lys358Arg)
18g.31536385A>TCA402142049DSG2c.1607A>T (p.Lys536Ile)
c.1073A>T (p.Lys358Ile)

Number of alleles fetched