Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.11758427G>ACA370315800GATA4c.1281G>A (p.Trp427Ter)
c.1284G>A (p.Trp428Ter)
n.726G>A
c.663G>A (p.Trp221Ter)
c.1278G>A (p.Trp426Ter)
c.537G>A (p.Trp179Ter)
 dbSNP
8g.11758427G>CCA370315801GATA4c.1281G>C (p.Trp427Cys)
c.1284G>C (p.Trp428Cys)
n.726G>C
c.663G>C (p.Trp221Cys)
c.1278G>C (p.Trp426Cys)
c.537G>C (p.Trp179Cys)
8g.11758427G=CA1764074315GATA4c.1281G= (p.Trp427=)
c.1284G= (p.Trp428=)
n.726G=
c.663G= (p.Trp221=)
c.1278G= (p.Trp426=)
c.537G= (p.Trp179=)
8g.11758427G>TCA370315802GATA4c.1281G>T (p.Trp427Cys)
c.1284G>T (p.Trp428Cys)
n.726G>T
c.663G>T (p.Trp221Cys)
c.1278G>T (p.Trp426Cys)
c.537G>T (p.Trp179Cys)
8g.11758428A=CA1764074321GATA4c.1282A= (p.Asn428=)
c.1285A= (p.Asn429=)
n.727A=
c.664A= (p.Asn222=)
c.1279A= (p.Asn427=)
c.538A= (p.Asn180=)
8g.11758428A>CCA370315803GATA4c.1282A>C (p.Asn428His)
c.1285A>C (p.Asn429His)
n.727A>C
c.664A>C (p.Asn222His)
c.1279A>C (p.Asn427His)
c.538A>C (p.Asn180His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758428A>GCA370315804GATA4c.1282A>G (p.Asn428Asp)
c.1285A>G (p.Asn429Asp)
n.727A>G
c.664A>G (p.Asn222Asp)
c.1279A>G (p.Asn427Asp)
c.538A>G (p.Asn180Asp)
8g.11758428A>TCA370315805GATA4c.1282A>T (p.Asn428Tyr)
c.1285A>T (p.Asn429Tyr)
n.727A>T
c.664A>T (p.Asn222Tyr)
c.1279A>T (p.Asn427Tyr)
c.538A>T (p.Asn180Tyr)
8g.11758429A=CA1764074327GATA4c.1283A= (p.Asn428=)
c.1286A= (p.Asn429=)
n.728A=
c.665A= (p.Asn222=)
c.1280A= (p.Asn427=)
c.539A= (p.Asn180=)
8g.11758429A>CCA172121516GATA4c.1283A>C (p.Asn428Thr)
c.1286A>C (p.Asn429Thr)
n.728A>C
c.665A>C (p.Asn222Thr)
c.1280A>C (p.Asn427Thr)
c.539A>C (p.Asn180Thr)
 dbSNP
8g.11758429A>GCA370315806GATA4c.1283A>G (p.Asn428Ser)
c.1286A>G (p.Asn429Ser)
n.728A>G
c.665A>G (p.Asn222Ser)
c.1280A>G (p.Asn427Ser)
c.539A>G (p.Asn180Ser)
 ClinVar dbSNP
8g.11758429A>TCA370315807GATA4c.1283A>T (p.Asn428Ile)
c.1286A>T (p.Asn429Ile)
n.728A>T
c.665A>T (p.Asn222Ile)
c.1280A>T (p.Asn427Ile)
c.539A>T (p.Asn180Ile)
8g.11758430C>ACA370315808GATA4c.1284C>A (p.Asn428Lys)
c.1287C>A (p.Asn429Lys)
n.729C>A
c.666C>A (p.Asn222Lys)
c.1281C>A (p.Asn427Lys)
c.540C>A (p.Asn180Lys)
8g.11758430C>GCA370315809GATA4c.1284C>G (p.Asn428Lys)
c.1287C>G (p.Asn429Lys)
n.729C>G
c.666C>G (p.Asn222Lys)
c.1281C>G (p.Asn427Lys)
c.540C>G (p.Asn180Lys)
8g.11758430C>TCA459314427GATA4c.1284C>T (p.Asn428=)
c.1287C>T (p.Asn429=)
n.729C>T
c.666C>T (p.Asn222=)
c.1281C>T (p.Asn427=)
c.540C>T (p.Asn180=)
 gnomAD v4
8g.11758431A=CA1764074331GATA4c.1285A= (p.Ser429=)
c.1288A= (p.Ser430=)
n.730A=
c.667A= (p.Ser223=)
c.1282A= (p.Ser428=)
c.541A= (p.Ser181=)
8g.11758431A>CCA370315810GATA4c.1285A>C (p.Ser429Arg)
c.1288A>C (p.Ser430Arg)
n.730A>C
c.667A>C (p.Ser223Arg)
c.1282A>C (p.Ser428Arg)
c.541A>C (p.Ser181Arg)
8g.11758431A>GCA4630902GATA4c.1285A>G (p.Ser429Gly)
c.1288A>G (p.Ser430Gly)
n.730A>G
c.667A>G (p.Ser223Gly)
c.1282A>G (p.Ser428Gly)
c.541A>G (p.Ser181Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758431A>TCA370315811GATA4c.1285A>T (p.Ser429Cys)
c.1288A>T (p.Ser430Cys)
n.730A>T
c.667A>T (p.Ser223Cys)
c.1282A>T (p.Ser428Cys)
c.541A>T (p.Ser181Cys)
8g.11758432G>ACA370315812GATA4c.1286G>A (p.Ser429Asn)
c.1289G>A (p.Ser430Asn)
n.731G>A
c.668G>A (p.Ser223Asn)
c.1283G>A (p.Ser428Asn)
c.542G>A (p.Ser181Asn)
 ClinVar
8g.11758432G>CCA370315813GATA4c.1286G>C (p.Ser429Thr)
c.1289G>C (p.Ser430Thr)
n.731G>C
c.668G>C (p.Ser223Thr)
c.1283G>C (p.Ser428Thr)
c.542G>C (p.Ser181Thr)
 gnomAD v4
8g.11758432G>TCA370315814GATA4c.1286G>T (p.Ser429Ile)
c.1289G>T (p.Ser430Ile)
n.731G>T
c.668G>T (p.Ser223Ile)
c.1283G>T (p.Ser428Ile)
c.542G>T (p.Ser181Ile)
8g.11758433C>ACA4630903GATA4c.1287C>A (p.Ser429Arg)
c.1290C>A (p.Ser430Arg)
n.732C>A
c.669C>A (p.Ser223Arg)
c.1284C>A (p.Ser428Arg)
c.543C>A (p.Ser181Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758433C=CA1764074335GATA4c.1287C= (p.Ser429=)
c.1290C= (p.Ser430=)
n.732C=
c.669C= (p.Ser223=)
c.1284C= (p.Ser428=)
c.543C= (p.Ser181=)
8g.11758433C>GCA370315815GATA4c.1287C>G (p.Ser429Arg)
c.1290C>G (p.Ser430Arg)
n.732C>G
c.669C>G (p.Ser223Arg)
c.1284C>G (p.Ser428Arg)
c.543C>G (p.Ser181Arg)
 dbSNP gnomAD v4
8g.11758433C>TCA172121521GATA4c.1287C>T (p.Ser429=)
c.1290C>T (p.Ser430=)
n.732C>T
c.669C>T (p.Ser223=)
c.1284C>T (p.Ser428=)
c.543C>T (p.Ser181=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
8g.11758434C>ACA370315816GATA4c.1288C>A (p.Leu430Met)
c.1291C>A (p.Leu431Met)
n.733C>A
c.670C>A (p.Leu224Met)
c.1285C>A (p.Leu429Met)
c.544C>A (p.Leu182Met)
8g.11758434C>GCA370315817GATA4c.1288C>G (p.Leu430Val)
c.1291C>G (p.Leu431Val)
n.733C>G
c.670C>G (p.Leu224Val)
c.1285C>G (p.Leu429Val)
c.544C>G (p.Leu182Val)
8g.11758434C>TCA459314449GATA4c.1288C>T (p.Leu430=)
c.1291C>T (p.Leu431=)
n.733C>T
c.670C>T (p.Leu224=)
c.1285C>T (p.Leu429=)
c.544C>T (p.Leu182=)
 gnomAD v4
8g.11758435T>ACA370315819GATA4c.1289T>A (p.Leu430Gln)
c.1292T>A (p.Leu431Gln)
n.734T>A
c.671T>A (p.Leu224Gln)
c.1286T>A (p.Leu429Gln)
c.545T>A (p.Leu182Gln)
8g.11758435T>CCA370315820GATA4c.1289T>C (p.Leu430Pro)
c.1292T>C (p.Leu431Pro)
n.734T>C
c.671T>C (p.Leu224Pro)
c.1286T>C (p.Leu429Pro)
c.545T>C (p.Leu182Pro)
 gnomAD v4
8g.11758435T>GCA370315818GATA4c.1289T>G (p.Leu430Arg)
c.1292T>G (p.Leu431Arg)
n.734T>G
c.671T>G (p.Leu224Arg)
c.1286T>G (p.Leu429Arg)
c.545T>G (p.Leu182Arg)
8g.11758436G>ACA459314457GATA4c.1290G>A (p.Leu430=)
c.1293G>A (p.Leu431=)
n.735G>A
c.672G>A (p.Leu224=)
c.1287G>A (p.Leu429=)
c.546G>A (p.Leu182=)
8g.11758436G>CCA459314459GATA4c.1290G>C (p.Leu430=)
c.1293G>C (p.Leu431=)
n.735G>C
c.672G>C (p.Leu224=)
c.1287G>C (p.Leu429=)
c.546G>C (p.Leu182=)
8g.11758436G>TCA459314460GATA4c.1290G>T (p.Leu430=)
c.1293G>T (p.Leu431=)
n.735G>T
c.672G>T (p.Leu224=)
c.1287G>T (p.Leu429=)
c.546G>T (p.Leu182=)
8g.11758437G>ACA370315821GATA4c.1291G>A (p.Val431Ile)
c.1294G>A (p.Val432Ile)
n.736G>A
c.673G>A (p.Val225Ile)
c.1288G>A (p.Val430Ile)
c.547G>A (p.Val183Ile)
8g.11758437G>CCA4630904GATA4c.1291G>C (p.Val431Leu)
c.1294G>C (p.Val432Leu)
n.736G>C
c.673G>C (p.Val225Leu)
c.1288G>C (p.Val430Leu)
c.547G>C (p.Val183Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758437G=CA1764074340GATA4c.1291G= (p.Val431=)
c.1294G= (p.Val432=)
n.736G=
c.673G= (p.Val225=)
c.1288G= (p.Val430=)
c.547G= (p.Val183=)
8g.11758437G>TCA370315822GATA4c.1291G>T (p.Val431Phe)
c.1294G>T (p.Val432Phe)
n.736G>T
c.673G>T (p.Val225Phe)
c.1288G>T (p.Val430Phe)
c.547G>T (p.Val183Phe)
8g.11758438T>ACA370315823GATA4c.1292T>A (p.Val431Asp)
c.1295T>A (p.Val432Asp)
n.737T>A
c.674T>A (p.Val225Asp)
c.1289T>A (p.Val430Asp)
c.548T>A (p.Val183Asp)
8g.11758438T>CCA370315824GATA4c.1292T>C (p.Val431Ala)
c.1295T>C (p.Val432Ala)
n.737T>C
c.674T>C (p.Val225Ala)
c.1289T>C (p.Val430Ala)
c.548T>C (p.Val183Ala)
8g.11758438T>GCA4630905GATA4c.1292T>G (p.Val431Gly)
c.1295T>G (p.Val432Gly)
n.737T>G
c.674T>G (p.Val225Gly)
c.1289T>G (p.Val430Gly)
c.548T>G (p.Val183Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758438T=CA1764074343GATA4c.1292T= (p.Val431=)
c.1295T= (p.Val432=)
n.737T=
c.674T= (p.Val225=)
c.1289T= (p.Val430=)
c.548T= (p.Val183=)
8g.11758439C>ACA459314476GATA4c.1293C>A (p.Val431=)
c.1296C>A (p.Val432=)
n.738C>A
c.675C>A (p.Val225=)
c.1290C>A (p.Val430=)
c.549C>A (p.Val183=)
 COSMIC
8g.11758439C=CA1764074348GATA4c.1293C= (p.Val431=)
c.1296C= (p.Val432=)
n.738C=
c.675C= (p.Val225=)
c.1290C= (p.Val430=)
c.549C= (p.Val183=)
8g.11758439C>GCA4630906GATA4c.1293C>G (p.Val431=)
c.1296C>G (p.Val432=)
n.738C>G
c.675C>G (p.Val225=)
c.1290C>G (p.Val430=)
c.549C>G (p.Val183=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758439C>TCA4630907GATA4c.1293C>T (p.Val431=)
c.1296C>T (p.Val432=)
n.738C>T
c.675C>T (p.Val225=)
c.1290C>T (p.Val430=)
c.549C>T (p.Val183=)
 dbSNP ExAC gnomAD v3 gnomAD v4
8g.11758440T>ACA370315825GATA4c.1294T>A (p.Leu432Met)
c.1297T>A (p.Leu433Met)
n.739T>A
c.676T>A (p.Leu226Met)
c.1291T>A (p.Leu431Met)
c.550T>A (p.Leu184Met)
8g.11758440T>CCA459314484GATA4c.1294T>C (p.Leu432=)
c.1297T>C (p.Leu433=)
n.739T>C
c.676T>C (p.Leu226=)
c.1291T>C (p.Leu431=)
c.550T>C (p.Leu184=)
 dbSNP
8g.11758440T>GCA370315826GATA4c.1294T>G (p.Leu432Val)
c.1297T>G (p.Leu433Val)
n.739T>G
c.676T>G (p.Leu226Val)
c.1291T>G (p.Leu431Val)
c.550T>G (p.Leu184Val)
8g.11758440T=CA1764074349GATA4c.1294T= (p.Leu432=)
c.1297T= (p.Leu433=)
n.739T=
c.676T= (p.Leu226=)
c.1291T= (p.Leu431=)
c.550T= (p.Leu184=)
8g.11758441T>ACA370315827GATA4c.1295T>A (p.Leu432Ter)
c.1298T>A (p.Leu433Ter)
n.740T>A
c.677T>A (p.Leu226Ter)
c.1292T>A (p.Leu431Ter)
c.551T>A (p.Leu184Ter)
8g.11758441T>CCA370315828GATA4c.1295T>C (p.Leu432Ser)
c.1298T>C (p.Leu433Ser)
n.740T>C
c.677T>C (p.Leu226Ser)
c.1292T>C (p.Leu431Ser)
c.551T>C (p.Leu184Ser)
8g.11758441T>GCA370315829GATA4c.1295T>G (p.Leu432Trp)
c.1298T>G (p.Leu433Trp)
n.740T>G
c.677T>G (p.Leu226Trp)
c.1292T>G (p.Leu431Trp)
c.551T>G (p.Leu184Trp)
8g.11758442G>ACA459314495GATA4c.1296G>A (p.Leu432=)
c.1299G>A (p.Leu433=)
n.741G>A
c.678G>A (p.Leu226=)
c.1293G>A (p.Leu431=)
c.552G>A (p.Leu184=)
8g.11758442G>CCA370315831GATA4c.1296G>C (p.Leu432Phe)
c.1299G>C (p.Leu433Phe)
n.741G>C
c.678G>C (p.Leu226Phe)
c.1293G>C (p.Leu431Phe)
c.552G>C (p.Leu184Phe)
8g.11758442G>TCA370315830GATA4c.1296G>T (p.Leu432Phe)
c.1299G>T (p.Leu433Phe)
n.741G>T
c.678G>T (p.Leu226Phe)
c.1293G>T (p.Leu431Phe)
c.552G>T (p.Leu184Phe)
8g.11758443G>ACA370315832GATA4c.1297G>A (p.Ala433Thr)
c.1300G>A (p.Ala434Thr)
n.742G>A
c.679G>A (p.Ala227Thr)
c.1294G>A (p.Ala432Thr)
c.553G>A (p.Ala185Thr)
 gnomAD v4
8g.11758443G>CCA370315833GATA4c.1297G>C (p.Ala433Pro)
c.1300G>C (p.Ala434Pro)
n.742G>C
c.679G>C (p.Ala227Pro)
c.1294G>C (p.Ala432Pro)
c.553G>C (p.Ala185Pro)
8g.11758443G>TCA370315834GATA4c.1297G>T (p.Ala433Ser)
c.1300G>T (p.Ala434Ser)
n.742G>T
c.679G>T (p.Ala227Ser)
c.1294G>T (p.Ala432Ser)
c.553G>T (p.Ala185Ser)
8g.11758444C>ACA370315835GATA4c.1298C>A (p.Ala433Asp)
c.1301C>A (p.Ala434Asp)
n.743C>A
c.680C>A (p.Ala227Asp)
c.1295C>A (p.Ala432Asp)
c.554C>A (p.Ala185Asp)
8g.11758444C=CA1764074353GATA4c.1298C= (p.Ala433=)
c.1301C= (p.Ala434=)
n.743C=
c.680C= (p.Ala227=)
c.1295C= (p.Ala432=)
c.554C= (p.Ala185=)
8g.11758444C>GCA370315836GATA4c.1298C>G (p.Ala433Gly)
c.1301C>G (p.Ala434Gly)
n.743C>G
c.680C>G (p.Ala227Gly)
c.1295C>G (p.Ala432Gly)
c.554C>G (p.Ala185Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
8g.11758444C>TCA370315837GATA4c.1298C>T (p.Ala433Val)
c.1301C>T (p.Ala434Val)
n.743C>T
c.680C>T (p.Ala227Val)
c.1295C>T (p.Ala432Val)
c.554C>T (p.Ala185Val)
8g.11758445C>ACA459314505GATA4c.1299C>A (p.Ala433=)
c.1302C>A (p.Ala434=)
n.744C>A
c.681C>A (p.Ala227=)
c.1296C>A (p.Ala432=)
c.555C>A (p.Ala185=)
8g.11758445C=CA1764074356GATA4c.1299C= (p.Ala433=)
c.1302C= (p.Ala434=)
n.744C=
c.681C= (p.Ala227=)
c.1296C= (p.Ala432=)
c.555C= (p.Ala185=)
8g.11758445C>GCA459314506GATA4c.1299C>G (p.Ala433=)
c.1302C>G (p.Ala434=)
n.744C>G
c.681C>G (p.Ala227=)
c.1296C>G (p.Ala432=)
c.555C>G (p.Ala185=)
8g.11758445C>TCA459314508GATA4c.1299C>T (p.Ala433=)
c.1302C>T (p.Ala434=)
n.744C>T
c.681C>T (p.Ala227=)
c.1296C>T (p.Ala432=)
c.555C>T (p.Ala185=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.11758446G>ACA4630908GATA4c.1300G>A (p.Asp434Asn)
c.1303G>A (p.Asp435Asn)
n.745G>A
c.682G>A (p.Asp228Asn)
c.1297G>A (p.Asp433Asn)
c.556G>A (p.Asp186Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758446G>CCA370315838GATA4c.1300G>C (p.Asp434His)
c.1303G>C (p.Asp435His)
n.745G>C
c.682G>C (p.Asp228His)
c.1297G>C (p.Asp433His)
c.556G>C (p.Asp186His)
8g.11758446G=CA1764074360GATA4c.1300G= (p.Asp434=)
c.1303G= (p.Asp435=)
n.745G=
c.682G= (p.Asp228=)
c.1297G= (p.Asp433=)
c.556G= (p.Asp186=)
8g.11758446G>TCA370315839GATA4c.1300G>T (p.Asp434Tyr)
c.1303G>T (p.Asp435Tyr)
n.745G>T
c.682G>T (p.Asp228Tyr)
c.1297G>T (p.Asp433Tyr)
c.556G>T (p.Asp186Tyr)
 dbSNP
8g.11758447A>CCA370315840GATA4c.1301A>C (p.Asp434Ala)
c.1304A>C (p.Asp435Ala)
n.746A>C
c.683A>C (p.Asp228Ala)
c.1298A>C (p.Asp433Ala)
c.557A>C (p.Asp186Ala)
8g.11758447A>GCA370315841GATA4c.1301A>G (p.Asp434Gly)
c.1304A>G (p.Asp435Gly)
n.746A>G
c.683A>G (p.Asp228Gly)
c.1298A>G (p.Asp433Gly)
c.557A>G (p.Asp186Gly)
8g.11758447A>TCA370315842GATA4c.1301A>T (p.Asp434Val)
c.1304A>T (p.Asp435Val)
n.746A>T
c.683A>T (p.Asp228Val)
c.1298A>T (p.Asp433Val)
c.557A>T (p.Asp186Val)
8g.11758448C>ACA370315843GATA4c.1302C>A (p.Asp434Glu)
c.1305C>A (p.Asp435Glu)
n.747C>A
c.684C>A (p.Asp228Glu)
c.1299C>A (p.Asp433Glu)
c.558C>A (p.Asp186Glu)
 gnomAD v4
8g.11758448C>GCA370315844GATA4c.1302C>G (p.Asp434Glu)
c.1305C>G (p.Asp435Glu)
n.747C>G
c.684C>G (p.Asp228Glu)
c.1299C>G (p.Asp433Glu)
c.558C>G (p.Asp186Glu)
8g.11758448C>TCA459314519GATA4c.1302C>T (p.Asp434=)
c.1305C>T (p.Asp435=)
n.747C>T
c.684C>T (p.Asp228=)
c.1299C>T (p.Asp433=)
c.558C>T (p.Asp186=)
 gnomAD v4
8g.11758449A=CA1764074363GATA4c.1303A= (p.Ser435=)
c.1306A= (p.Ser436=)
n.748A=
c.685A= (p.Ser229=)
c.1300A= (p.Ser434=)
c.559A= (p.Ser187=)
8g.11758449A>CCA172121538GATA4c.1303A>C (p.Ser435Arg)
c.1306A>C (p.Ser436Arg)
n.748A>C
c.685A>C (p.Ser229Arg)
c.1300A>C (p.Ser434Arg)
c.559A>C (p.Ser187Arg)
 dbSNP gnomAD v3 gnomAD v4
8g.11758449A>GCA370315846GATA4c.1303A>G (p.Ser435Gly)
c.1306A>G (p.Ser436Gly)
n.748A>G
c.685A>G (p.Ser229Gly)
c.1300A>G (p.Ser434Gly)
c.559A>G (p.Ser187Gly)
 dbSNP
8g.11758449A>TCA370315845GATA4c.1303A>T (p.Ser435Cys)
c.1306A>T (p.Ser436Cys)
n.748A>T
c.685A>T (p.Ser229Cys)
c.1300A>T (p.Ser434Cys)
c.559A>T (p.Ser187Cys)
8g.11758450G>ACA370315847GATA4c.1304G>A (p.Ser435Asn)
c.1307G>A (p.Ser436Asn)
n.749G>A
c.686G>A (p.Ser229Asn)
c.1301G>A (p.Ser434Asn)
c.560G>A (p.Ser187Asn)
8g.11758450G>CCA370315848GATA4c.1304G>C (p.Ser435Thr)
c.1307G>C (p.Ser436Thr)
n.749G>C
c.686G>C (p.Ser229Thr)
c.1301G>C (p.Ser434Thr)
c.560G>C (p.Ser187Thr)
8g.11758450G>TCA370315849GATA4c.1304G>T (p.Ser435Ile)
c.1307G>T (p.Ser436Ile)
n.749G>T
c.686G>T (p.Ser229Ile)
c.1301G>T (p.Ser434Ile)
c.560G>T (p.Ser187Ile)
8g.11758451T>ACA4630909GATA4c.1305T>A (p.Ser435Arg)
c.1308T>A (p.Ser436Arg)
n.750T>A
c.687T>A (p.Ser229Arg)
c.1302T>A (p.Ser434Arg)
c.561T>A (p.Ser187Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758451T>CCA459314528GATA4c.1305T>C (p.Ser435=)
c.1308T>C (p.Ser436=)
n.750T>C
c.687T>C (p.Ser229=)
c.1302T>C (p.Ser434=)
c.561T>C (p.Ser187=)
 dbSNP gnomAD v3 gnomAD v4
8g.11758451T>GCA370315850GATA4c.1305T>G (p.Ser435Arg)
c.1308T>G (p.Ser436Arg)
n.750T>G
c.687T>G (p.Ser229Arg)
c.1302T>G (p.Ser434Arg)
c.561T>G (p.Ser187Arg)
8g.11758451T=CA1764074367GATA4c.1305T= (p.Ser435=)
c.1308T= (p.Ser436=)
n.750T=
c.687T= (p.Ser229=)
c.1302T= (p.Ser434=)
c.561T= (p.Ser187=)
8g.11758452C>ACA370315853GATA4c.1306C>A (p.His436Asn)
c.1309C>A (p.His437Asn)
n.751C>A
c.688C>A (p.His230Asn)
c.1303C>A (p.His435Asn)
c.562C>A (p.His188Asn)
8g.11758452C>GCA370315852GATA4c.1306C>G (p.His436Asp)
c.1309C>G (p.His437Asp)
n.751C>G
c.688C>G (p.His230Asp)
c.1303C>G (p.His435Asp)
c.562C>G (p.His188Asp)
 gnomAD v4
8g.11758452C>TCA370315851GATA4c.1306C>T (p.His436Tyr)
c.1309C>T (p.His437Tyr)
n.751C>T
c.688C>T (p.His230Tyr)
c.1303C>T (p.His435Tyr)
c.562C>T (p.His188Tyr)
8g.11758453A>CCA370315854GATA4c.1307A>C (p.His436Pro)
c.1310A>C (p.His437Pro)
n.752A>C
c.689A>C (p.His230Pro)
c.1304A>C (p.His435Pro)
c.563A>C (p.His188Pro)
8g.11758453A>GCA370315855GATA4c.1307A>G (p.His436Arg)
c.1310A>G (p.His437Arg)
n.752A>G
c.689A>G (p.His230Arg)
c.1304A>G (p.His435Arg)
c.563A>G (p.His188Arg)
8g.11758453A>TCA370315856GATA4c.1307A>T (p.His436Leu)
c.1310A>T (p.His437Leu)
n.752A>T
c.689A>T (p.His230Leu)
c.1304A>T (p.His435Leu)
c.563A>T (p.His188Leu)
8g.11758454C>ACA370315857GATA4c.1308C>A (p.His436Gln)
c.1311C>A (p.His437Gln)
n.753C>A
c.690C>A (p.His230Gln)
c.1305C>A (p.His435Gln)
c.564C>A (p.His188Gln)
 ClinVar dbSNP gnomAD v3 gnomAD v4
8g.11758454C=CA1764074373GATA4c.1308C= (p.His436=)
c.1311C= (p.His437=)
n.753C=
c.690C= (p.His230=)
c.1305C= (p.His435=)
c.564C= (p.His188=)
8g.11758454C>GCA370315858GATA4c.1308C>G (p.His436Gln)
c.1311C>G (p.His437Gln)
n.753C>G
c.690C>G (p.His230Gln)
c.1305C>G (p.His435Gln)
c.564C>G (p.His188Gln)
 ClinVar dbSNP
8g.11758454C>TCA4630910GATA4c.1308C>T (p.His436=)
c.1311C>T (p.His437=)
n.753C>T
c.690C>T (p.His230=)
c.1305C>T (p.His435=)
c.564C>T (p.His188=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758455G>ACA370315860GATA4c.1309G>A (p.Gly437Arg)
c.1312G>A (p.Gly438Arg)
n.754G>A
c.691G>A (p.Gly231Arg)
c.1306G>A (p.Gly436Arg)
c.565G>A (p.Gly189Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758455G>CCA370315859GATA4c.1309G>C (p.Gly437Arg)
c.1312G>C (p.Gly438Arg)
n.754G>C
c.691G>C (p.Gly231Arg)
c.1306G>C (p.Gly436Arg)
c.565G>C (p.Gly189Arg)
8g.11758455G=CA1764074377GATA4c.1309G= (p.Gly437=)
c.1312G= (p.Gly438=)
n.754G=
c.691G= (p.Gly231=)
c.1306G= (p.Gly436=)
c.565G= (p.Gly189=)
8g.11758455G>TCA4630911GATA4c.1309G>T (p.Gly437Trp)
c.1312G>T (p.Gly438Trp)
n.754G>T
c.691G>T (p.Gly231Trp)
c.1306G>T (p.Gly436Trp)
c.565G>T (p.Gly189Trp)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758456G>ACA370315861GATA4c.1310G>A (p.Gly437Glu)
c.1313G>A (p.Gly438Glu)
n.755G>A
c.692G>A (p.Gly231Glu)
c.1307G>A (p.Gly436Glu)
c.566G>A (p.Gly189Glu)
8g.11758456G>CCA370315862GATA4c.1310G>C (p.Gly437Ala)
c.1313G>C (p.Gly438Ala)
n.755G>C
c.692G>C (p.Gly231Ala)
c.1307G>C (p.Gly436Ala)
c.566G>C (p.Gly189Ala)
8g.11758456G>TCA370315863GATA4c.1310G>T (p.Gly437Val)
c.1313G>T (p.Gly438Val)
n.755G>T
c.692G>T (p.Gly231Val)
c.1307G>T (p.Gly436Val)
c.566G>T (p.Gly189Val)
8g.11758457G>ACA459314550GATA4c.1311G>A (p.Gly437=)
c.1314G>A (p.Gly438=)
n.756G>A
c.693G>A (p.Gly231=)
c.1308G>A (p.Gly436=)
c.567G>A (p.Gly189=)
 ClinVar gnomAD v4
8g.11758457G>CCA459314551GATA4c.1311G>C (p.Gly437=)
c.1314G>C (p.Gly438=)
n.756G>C
c.693G>C (p.Gly231=)
c.1308G>C (p.Gly436=)
c.567G>C (p.Gly189=)
8g.11758457G>TCA459314553GATA4c.1311G>T (p.Gly437=)
c.1314G>T (p.Gly438=)
n.756G>T
c.693G>T (p.Gly231=)
c.1308G>T (p.Gly436=)
c.567G>T (p.Gly189=)
 gnomAD v4
8g.11758458G>ACA16618586GATA4c.1312G>A (p.Asp438Asn)
c.1315G>A (p.Asp439Asn)
n.757G>A
c.694G>A (p.Asp232Asn)
c.1309G>A (p.Asp437Asn)
c.568G>A (p.Asp190Asn)
 ClinVar dbSNP COSMIC
8g.11758458G>CCA370315864GATA4c.1312G>C (p.Asp438His)
c.1315G>C (p.Asp439His)
n.757G>C
c.694G>C (p.Asp232His)
c.1309G>C (p.Asp437His)
c.568G>C (p.Asp190His)
 ClinVar dbSNP
8g.11758458G=CA1764074387GATA4c.1312G= (p.Asp438=)
c.1315G= (p.Asp439=)
n.757G=
c.694G= (p.Asp232=)
c.1309G= (p.Asp437=)
c.568G= (p.Asp190=)
8g.11758458G>TCA172121549GATA4c.1312G>T (p.Asp438Tyr)
c.1315G>T (p.Asp439Tyr)
n.757G>T
c.694G>T (p.Asp232Tyr)
c.1309G>T (p.Asp437Tyr)
c.568G>T (p.Asp190Tyr)
 dbSNP gnomAD v4
8g.11758459A>CCA370315867GATA4c.1313A>C (p.Asp438Ala)
c.1316A>C (p.Asp439Ala)
n.758A>C
c.695A>C (p.Asp232Ala)
c.1310A>C (p.Asp437Ala)
c.569A>C (p.Asp190Ala)
8g.11758459A>GCA370315865GATA4c.1313A>G (p.Asp438Gly)
c.1316A>G (p.Asp439Gly)
n.758A>G
c.695A>G (p.Asp232Gly)
c.1310A>G (p.Asp437Gly)
c.569A>G (p.Asp190Gly)
8g.11758459A>TCA370315866GATA4c.1313A>T (p.Asp438Val)
c.1316A>T (p.Asp439Val)
n.758A>T
c.695A>T (p.Asp232Val)
c.1310A>T (p.Asp437Val)
c.569A>T (p.Asp190Val)
8g.11758460C>ACA370315868GATA4c.1314C>A (p.Asp438Glu)
c.1317C>A (p.Asp439Glu)
n.759C>A
c.696C>A (p.Asp232Glu)
c.1311C>A (p.Asp437Glu)
c.570C>A (p.Asp190Glu)
8g.11758460C=CA1764074391GATA4c.1314C= (p.Asp438=)
c.1317C= (p.Asp439=)
n.759C=
c.696C= (p.Asp232=)
c.1311C= (p.Asp437=)
c.570C= (p.Asp190=)
8g.11758460C>GCA370315869GATA4c.1314C>G (p.Asp438Glu)
c.1317C>G (p.Asp439Glu)
n.759C>G
c.696C>G (p.Asp232Glu)
c.1311C>G (p.Asp437Glu)
c.570C>G (p.Asp190Glu)
8g.11758460C>TCA459314561GATA4c.1314C>T (p.Asp438=)
c.1317C>T (p.Asp439=)
n.759C>T
c.696C>T (p.Asp232=)
c.1311C>T (p.Asp437=)
c.570C>T (p.Asp190=)
8g.11758461A=CA1764074395GATA4c.1315A= (p.Ile439=)
c.1318A= (p.Ile440=)
n.760A=
c.697A= (p.Ile233=)
c.1312A= (p.Ile438=)
c.571A= (p.Ile191=)
8g.11758461A>CCA370315870GATA4c.1315A>C (p.Ile439Leu)
c.1318A>C (p.Ile440Leu)
n.760A>C
c.697A>C (p.Ile233Leu)
c.1312A>C (p.Ile438Leu)
c.571A>C (p.Ile191Leu)
8g.11758461A>GCA4630912GATA4c.1315A>G (p.Ile439Val)
c.1318A>G (p.Ile440Val)
n.760A>G
c.697A>G (p.Ile233Val)
c.1312A>G (p.Ile438Val)
c.571A>G (p.Ile191Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758461A>TCA370315871GATA4c.1315A>T (p.Ile439Leu)
c.1318A>T (p.Ile440Leu)
n.760A>T
c.697A>T (p.Ile233Leu)
c.1312A>T (p.Ile438Leu)
c.571A>T (p.Ile191Leu)
 ClinVar dbSNP gnomAD v4
8g.11758462_11758463dupCA1110747662GATA4c.1316_1317dup (p.Ile440Ter)
c.1319_1320dup (p.Ile441Ter)
n.761_762dup
c.698_699dup (p.Ile234Ter)
c.1313_1314dup (p.Ile439Ter)
c.572_573dup (p.Ile192Ter)
 dbSNP gnomAD v3 gnomAD v4
8g.11758462T>ACA370315872GATA4c.1316T>A (p.Ile439Lys)
c.1319T>A (p.Ile440Lys)
n.761T>A
c.698T>A (p.Ile233Lys)
c.1313T>A (p.Ile438Lys)
c.572T>A (p.Ile191Lys)
 dbSNP gnomAD v3 gnomAD v4
8g.11758462T>CCA172121557GATA4c.1316T>C (p.Ile439Thr)
c.1319T>C (p.Ile440Thr)
n.761T>C
c.698T>C (p.Ile233Thr)
c.1313T>C (p.Ile438Thr)
c.572T>C (p.Ile191Thr)
 dbSNP gnomAD v2 gnomAD v4
8g.11758462T>GCA370315873GATA4c.1316T>G (p.Ile439Arg)
c.1319T>G (p.Ile440Arg)
n.761T>G
c.698T>G (p.Ile233Arg)
c.1313T>G (p.Ile438Arg)
c.572T>G (p.Ile191Arg)
8g.11758462T=CA1764074399GATA4c.1316T= (p.Ile439=)
c.1319T= (p.Ile440=)
n.761T=
c.698T= (p.Ile233=)
c.1313T= (p.Ile438=)
c.572T= (p.Ile191=)
8g.11758463A>CCA459314570GATA4c.1317A>C (p.Ile439=)
c.1320A>C (p.Ile440=)
n.762A>C
c.699A>C (p.Ile233=)
c.1314A>C (p.Ile438=)
c.573A>C (p.Ile191=)
8g.11758463A>GCA370315874GATA4c.1317A>G (p.Ile439Met)
c.1320A>G (p.Ile440Met)
n.762A>G
c.699A>G (p.Ile233Met)
c.1314A>G (p.Ile438Met)
c.573A>G (p.Ile191Met)
8g.11758463A>TCA459314572GATA4c.1317A>T (p.Ile439=)
c.1320A>T (p.Ile440=)
n.762A>T
c.699A>T (p.Ile233=)
c.1314A>T (p.Ile438=)
c.573A>T (p.Ile191=)
8g.11758464A>CCA370315875GATA4c.1318A>C (p.Ile440Leu)
c.1321A>C (p.Ile441Leu)
n.763A>C
c.700A>C (p.Ile234Leu)
c.1315A>C (p.Ile439Leu)
c.574A>C (p.Ile192Leu)
8g.11758464A>GCA370315876GATA4c.1318A>G (p.Ile440Val)
c.1321A>G (p.Ile441Val)
n.763A>G
c.700A>G (p.Ile234Val)
c.1315A>G (p.Ile439Val)
c.574A>G (p.Ile192Val)
 ClinVar dbSNP
8g.11758464A>TCA370315877GATA4c.1318A>T (p.Ile440Phe)
c.1321A>T (p.Ile441Phe)
n.763A>T
c.700A>T (p.Ile234Phe)
c.1315A>T (p.Ile439Phe)
c.574A>T (p.Ile192Phe)
8g.11758465T>ACA370315878GATA4c.1319T>A (p.Ile440Asn)
c.1322T>A (p.Ile441Asn)
n.764T>A
c.701T>A (p.Ile234Asn)
c.1316T>A (p.Ile439Asn)
c.575T>A (p.Ile192Asn)
 gnomAD v4
8g.11758465T>CCA370315879GATA4c.1319T>C (p.Ile440Thr)
c.1322T>C (p.Ile441Thr)
n.764T>C
c.701T>C (p.Ile234Thr)
c.1316T>C (p.Ile439Thr)
c.575T>C (p.Ile192Thr)
8g.11758465T>GCA370315880GATA4c.1319T>G (p.Ile440Ser)
c.1322T>G (p.Ile441Ser)
n.764T>G
c.701T>G (p.Ile234Ser)
c.1316T>G (p.Ile439Ser)
c.575T>G (p.Ile192Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
8g.11758466C>ACA459314580GATA4c.1320C>A (p.Ile440=)
c.1323C>A (p.Ile441=)
n.765C>A
c.702C>A (p.Ile234=)
c.1317C>A (p.Ile439=)
c.576C>A (p.Ile192=)
 gnomAD v4
8g.11758466C=CA1764074401GATA4c.1320C= (p.Ile440=)
c.1323C= (p.Ile441=)
n.765C=
c.702C= (p.Ile234=)
c.1317C= (p.Ile439=)
c.576C= (p.Ile192=)
8g.11758466C>GCA370315881GATA4c.1320C>G (p.Ile440Met)
c.1323C>G (p.Ile441Met)
n.765C>G
c.702C>G (p.Ile234Met)
c.1317C>G (p.Ile439Met)
c.576C>G (p.Ile192Met)
 dbSNP gnomAD v2 gnomAD v4
8g.11758466C>TCA459314581GATA4c.1320C>T (p.Ile440=)
c.1323C>T (p.Ile441=)
n.765C>T
c.702C>T (p.Ile234=)
c.1317C>T (p.Ile439=)
c.576C>T (p.Ile192=)
 gnomAD v4
8g.11758467A>CCA370315882GATA4c.1321A>C (p.Thr441Pro)
c.1324A>C (p.Thr442Pro)
n.766A>C
c.703A>C (p.Thr235Pro)
c.1318A>C (p.Thr440Pro)
c.577A>C (p.Thr193Pro)
8g.11758467A>GCA370315883GATA4c.1321A>G (p.Thr441Ala)
c.1324A>G (p.Thr442Ala)
n.766A>G
c.703A>G (p.Thr235Ala)
c.1318A>G (p.Thr440Ala)
c.577A>G (p.Thr193Ala)
8g.11758467A>TCA370315884GATA4c.1321A>T (p.Thr441Ser)
c.1324A>T (p.Thr442Ser)
n.766A>T
c.703A>T (p.Thr235Ser)
c.1318A>T (p.Thr440Ser)
c.577A>T (p.Thr193Ser)
8g.11758468C>ACA370315885GATA4c.1322C>A (p.Thr441Asn)
c.1325C>A (p.Thr442Asn)
n.767C>A
c.704C>A (p.Thr235Asn)
c.1319C>A (p.Thr440Asn)
c.578C>A (p.Thr193Asn)
8g.11758468C=CA1764074406GATA4c.1322C= (p.Thr441=)
c.1325C= (p.Thr442=)
n.767C=
c.704C= (p.Thr235=)
c.1319C= (p.Thr440=)
c.578C= (p.Thr193=)
8g.11758468C>GCA4630913GATA4c.1322C>G (p.Thr441Ser)
c.1325C>G (p.Thr442Ser)
n.767C>G
c.704C>G (p.Thr235Ser)
c.1319C>G (p.Thr440Ser)
c.578C>G (p.Thr193Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758468C>TCA370315886GATA4c.1322C>T (p.Thr441Ile)
c.1325C>T (p.Thr442Ile)
n.767C>T
c.704C>T (p.Thr235Ile)
c.1319C>T (p.Thr440Ile)
c.578C>T (p.Thr193Ile)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758469T>ACA459314591GATA4c.1323T>A (p.Thr441=)
c.1326T>A (p.Thr442=)
n.768T>A
c.705T>A (p.Thr235=)
c.1320T>A (p.Thr440=)
c.579T>A (p.Thr193=)
8g.11758469T>CCA172121563GATA4c.1323T>C (p.Thr441=)
c.1326T>C (p.Thr442=)
n.768T>C
c.705T>C (p.Thr235=)
c.1320T>C (p.Thr440=)
c.579T>C (p.Thr193=)
 dbSNP
8g.11758469T>GCA459314595GATA4c.1323T>G (p.Thr441=)
c.1326T>G (p.Thr442=)
n.768T>G
c.705T>G (p.Thr235=)
c.1320T>G (p.Thr440=)
c.579T>G (p.Thr193=)
8g.11758469T=CA1764074409GATA4c.1323T= (p.Thr441=)
c.1326T= (p.Thr442=)
n.768T=
c.705T= (p.Thr235=)
c.1320T= (p.Thr440=)
c.579T= (p.Thr193=)
8g.11758470G>ACA370315887GATA4c.1324G>A (p.Ala442Thr)
c.1327G>A (p.Ala443Thr)
n.769G>A
c.706G>A (p.Ala236Thr)
c.1321G>A (p.Ala441Thr)
c.580G>A (p.Ala194Thr)
 dbSNP gnomAD v3 gnomAD v4
8g.11758470G>CCA370315888GATA4c.1324G>C (p.Ala442Pro)
c.1327G>C (p.Ala443Pro)
n.769G>C
c.706G>C (p.Ala236Pro)
c.1321G>C (p.Ala441Pro)
c.580G>C (p.Ala194Pro)
8g.11758470G=CA1764074413GATA4c.1324G= (p.Ala442=)
c.1327G= (p.Ala443=)
n.769G=
c.706G= (p.Ala236=)
c.1321G= (p.Ala441=)
c.580G= (p.Ala194=)
8g.11758470G>TCA370315889GATA4c.1324G>T (p.Ala442Ser)
c.1327G>T (p.Ala443Ser)
n.769G>T
c.706G>T (p.Ala236Ser)
c.1321G>T (p.Ala441Ser)
c.580G>T (p.Ala194Ser)
8g.11758471C>ACA370315890GATA4c.1325C>A (p.Ala442Glu)
c.1328C>A (p.Ala443Glu)
n.770C>A
c.707C>A (p.Ala236Glu)
c.1322C>A (p.Ala441Glu)
c.581C>A (p.Ala194Glu)
8g.11758471C=CA1764074420GATA4c.1325C= (p.Ala442=)
c.1328C= (p.Ala443=)
n.770C=
c.707C= (p.Ala236=)
c.1322C= (p.Ala441=)
c.581C= (p.Ala194=)
8g.11758471C>GCA4630914GATA4c.1325C>G (p.Ala442Gly)
c.1328C>G (p.Ala443Gly)
n.770C>G
c.707C>G (p.Ala236Gly)
c.1322C>G (p.Ala441Gly)
c.581C>G (p.Ala194Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758471C>TCA212672GATA4c.1325C>T (p.Ala442Val)
c.1328C>T (p.Ala443Val)
n.770C>T
c.707C>T (p.Ala236Val)
c.1322C>T (p.Ala441Val)
c.581C>T (p.Ala194Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758472G>ACA4630915GATA4c.1326G>A (p.Ala442=)
c.1329G>A (p.Ala443=)
n.771G>A
c.708G>A (p.Ala236=)
c.1323G>A (p.Ala441=)
c.582G>A (p.Ala194=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.11758472G>CCA459314605GATA4c.1326G>C (p.Ala442=)
c.1329G>C (p.Ala443=)
n.771G>C
c.708G>C (p.Ala236=)
c.1323G>C (p.Ala441=)
c.582G>C (p.Ala194=)
8g.11758472G=CA1764074428GATA4c.1326G= (p.Ala442=)
c.1329G= (p.Ala443=)
n.771G=
c.708G= (p.Ala236=)
c.1323G= (p.Ala441=)
c.582G= (p.Ala194=)
8g.11758472G>TCA459314606GATA4c.1326G>T (p.Ala442=)
c.1329G>T (p.Ala443=)
n.771G>T
c.708G>T (p.Ala236=)
c.1323G>T (p.Ala441=)
c.582G>T (p.Ala194=)
 gnomAD v4 COSMIC
8g.11758473T>ACA370315891GATA4c.1327T>A (p.Ter443Lys)
c.1330T>A (p.Ter444Lys)
n.772T>A
c.709T>A (p.Ter237Lys)
c.1324T>A (p.Ter442Lys)
c.583T>A (p.Ter195Lys)
8g.11758473T>CCA370315892GATA4c.1327T>C (p.Ter443Gln)
c.1330T>C (p.Ter444Gln)
n.772T>C
c.709T>C (p.Ter237Gln)
c.1324T>C (p.Ter442Gln)
c.583T>C (p.Ter195Gln)
8g.11758473T>GCA370315893GATA4c.1327T>G (p.Ter443Glu)
c.1330T>G (p.Ter444Glu)
n.772T>G
c.709T>G (p.Ter237Glu)
c.1324T>G (p.Ter442Glu)
c.583T>G (p.Ter195Glu)
8g.11758474A>CCA370315894GATA4c.1328A>C (p.Ter443Ser)
c.1331A>C (p.Ter444Ser)
n.773A>C
c.710A>C (p.Ter237Ser)
c.1325A>C (p.Ter442Ser)
c.584A>C (p.Ter195Ser)
8g.11758474A>GCA459314613GATA4c.1328A>G (p.Ter443=)
c.1331A>G (p.Ter444=)
n.773A>G
c.710A>G (p.Ter237=)
c.1325A>G (p.Ter442=)
c.584A>G (p.Ter195=)
8g.11758474A>TCA370315895GATA4c.1328A>T (p.Ter443Leu)
c.1331A>T (p.Ter444Leu)
n.773A>T
c.710A>T (p.Ter237Leu)
c.1325A>T (p.Ter442Leu)
c.584A>T (p.Ter195Leu)
8g.11758475A=CA1764074433GATA4c.1329A= (p.Ter443=)
c.1332A= (p.Ter444=)
n.774A=
c.711A= (p.Ter237=)
c.1326A= (p.Ter442=)
c.585A= (p.Ter195=)
8g.11758475A>CCA370315896GATA4c.1329A>C (p.Ter443Tyr)
c.1332A>C (p.Ter444Tyr)
n.774A>C
c.711A>C (p.Ter237Tyr)
c.1326A>C (p.Ter442Tyr)
c.585A>C (p.Ter195Tyr)
8g.11758475A>GCA459314618GATA4c.1329A>G (p.Ter443=)
c.1332A>G (p.Ter444=)
n.774A>G
c.711A>G (p.Ter237=)
c.1326A>G (p.Ter442=)
c.585A>G (p.Ter195=)
 gnomAD v4
8g.11758475A>TCA370315897GATA4c.1329A>T (p.Ter443Tyr)
c.1332A>T (p.Ter444Tyr)
n.774A>T
c.711A>T (p.Ter237Tyr)
c.1326A>T (p.Ter442Tyr)
c.585A>T (p.Ter195Tyr)
8g.11758476T>ACA2579094231GATA4c.*1T>A (n.*1T>A)
n.775T>A
c.1327T>A (n.1327T>A)
8g.11758476T>CCA846164205GATA4c.*1T>C (n.*1T>C)
n.775T>C
c.1327T>C (n.1327T>C)
 dbSNP
8g.11758476T=CA1764074436GATA4c.*1T= (n.*1T=)
n.775T=
c.1327T= (n.1327T=)
8g.11758485_11758491dupCA580031760GATA4c.*10_*16dup (n.*10_*16dup)
n.784_790dup
c.1336_1342dup (n.1336_1342dup)
 dbSNP gnomAD v2 gnomAD v4
8g.11758477C>ACA2579094232GATA4c.*2C>A (n.*2C>A)
n.776C>A
c.1328C>A (n.1328C>A)
 gnomAD v4
8g.11758477C=CA1764074437GATA4c.*2C= (n.*2C=)
n.776C=
c.1328C= (n.1328C=)
8g.11758477C>GCA4630916GATA4c.*2C>G (n.*2C>G)
n.776C>G
c.1328C>G (n.1328C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758478T>CCA2686137417GATA4c.*3T>C (n.*3T>C)
n.777T>C
c.1329T>C (n.1329T>C)
 gnomAD v4
8g.11758479T>CCA4630917GATA4c.*4T>C (n.*4T>C)
n.778T>C
c.1330T>C (n.1330T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758479T>GCA4630918GATA4c.*4T>G (n.*4T>G)
n.778T>G
c.1330T>G (n.1330T>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758479T=CA1764074439GATA4c.*4T= (n.*4T=)
n.778T=
c.1330T= (n.1330T=)
8g.11758480C=CA1764074441GATA4c.*5C= (n.*5C=)
n.779C=
c.1331C= (n.1331C=)
8g.11758480C>TCA172121581GATA4c.*5C>T (n.*5C>T)
n.779C>T
c.1331C>T (n.1331C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758481C=CA1764074444GATA4c.*6C= (n.*6C=)
n.780C=
c.1332C= (n.1332C=)
8g.11758481C>TCA4630919GATA4c.*6C>T (n.*6C>T)
n.780C>T
c.1332C>T (n.1332C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758482C=CA1764074447GATA4c.*7C= (n.*7C=)
n.781C=
c.1333C= (n.1333C=)
8g.11758482C>GCA172121583GATA4c.*7C>G (n.*7C>G)
n.781C>G
c.1333C>G (n.1333C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758482C>TCA1764074448GATA4c.*7C>T (n.*7C>T)
n.781C>T
c.1333C>T (n.1333C>T)
 dbSNP gnomAD v4
8g.11758484C>ACA4630921GATA4c.*9C>A (n.*9C>A)
n.783C>A
c.1335C>A (n.1335C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758484C=CA1764074451GATA4c.*9C= (n.*9C=)
n.783C=
c.1335C= (n.1335C=)
8g.11758484C>GCA172121588GATA4c.*9C>G (n.*9C>G)
n.783C>G
c.1335C>G (n.1335C>G)
 dbSNP gnomAD v4
8g.11758484C>TCA4630920GATA4c.*9C>T (n.*9C>T)
n.783C>T
c.1335C>T (n.1335C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758485T>CCA580031761GATA4c.*10T>C (n.*10T>C)
n.784T>C
c.1336T>C (n.1336T>C)
 dbSNP gnomAD v2 gnomAD v4
8g.11758485T=CA1764074454GATA4c.*10T= (n.*10T=)
n.784T=
c.1336T= (n.1336T=)
8g.11758486dupCA652201252GATA4c.*11dup (n.*11dup)
n.785dup
c.1337dup (n.1337dup)
8g.11758487C=CA1764074460GATA4c.*12C= (n.*12C=)
n.786C=
c.1338C= (n.1338C=)
8g.11758487C>GCA846164228GATA4c.*12C>G (n.*12C>G)
n.786C>G
c.1338C>G (n.1338C>G)
 dbSNP gnomAD v3 gnomAD v4
8g.11758487C>TCA4630922GATA4c.*12C>T (n.*12C>T)
n.786C>T
c.1338C>T (n.1338C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758487_11758490delinsCCCTCA1764074458GATA4c.*12_*15delinsCCCT (n.*12_*15delinsCCCT)
n.786_789delinsCCCT
c.1338_1341delinsCCCT (n.1338_1341delinsCCCT)
8g.11758488C>ACA2579094233GATA4c.*13C>A (n.*13C>A)
n.787C>A
c.1339C>A (n.1339C>A)
8g.11758492_11758494delCA1110747700GATA4c.*17_*19del (n.*17_*19del)
n.791_793del
c.1343_1345del (n.1343_1345del)
 dbSNP gnomAD v3 gnomAD v4
8g.11758489C>ACA2579094234GATA4c.*14C>A (n.*14C>A)
n.788C>A
c.1340C>A (n.1340C>A)
8g.11758489C=CA1764074465GATA4c.*14C= (n.*14C=)
n.788C=
c.1340C= (n.1340C=)
8g.11758489C>GCA1764074466GATA4c.*14C>G (n.*14C>G)
n.788C>G
c.1340C>G (n.1340C>G)
 dbSNP gnomAD v4
8g.11758490T>ACA2686137429GATA4c.*15T>A (n.*15T>A)
n.789T>A
c.1341T>A (n.1341T>A)
 gnomAD v4
8g.11758492C>ACA2686137430GATA4c.*17C>A (n.*17C>A)
n.791C>A
c.1343C>A (n.1343C>A)
 gnomAD v4
8g.11758492C=CA1764074469GATA4c.*17C= (n.*17C=)
n.791C=
c.1343C= (n.1343C=)
8g.11758492C>TCA580031762GATA4c.*17C>T (n.*17C>T)
n.791C>T
c.1343C>T (n.1343C>T)
 dbSNP gnomAD v2 gnomAD v4
8g.11758494C=CA1764074471GATA4c.*19C= (n.*19C=)
n.793C=
c.1345C= (n.1345C=)
8g.11758494C>GCA4630923GATA4c.*19C>G (n.*19C>G)
n.793C>G
c.1345C>G (n.1345C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758495A>TCA2686137431GATA4c.*20A>T (n.*20A>T)
n.794A>T
c.1346A>T (n.1346A>T)
 gnomAD v4
8g.11758496A>CCA2686137432GATA4c.*21A>C (n.*21A>C)
n.795A>C
c.1347A>C (n.1347A>C)
 gnomAD v4
8g.11758499T>CCA2686137433GATA4c.*24T>C (n.*24T>C)
n.798T>C
c.1350T>C (n.1350T>C)
 gnomAD v4
8g.11758500C>GCA2716590670GATA4c.*25C>G (n.*25C>G)
n.799C>G
c.1351C>G (n.1351C>G)
 dbSNP
8g.11758501C=CA1764074472GATA4c.*26C= (n.*26C=)
n.800C=
c.1352C= (n.1352C=)
8g.11758501C>GCA2579094235GATA4c.*26C>G (n.*26C>G)
n.800C>G
c.1352C>G (n.1352C>G)
8g.11758501C>TCA580031763GATA4c.*26C>T (n.*26C>T)
n.800C>T
c.1352C>T (n.1352C>T)
 dbSNP gnomAD v2 gnomAD v4
8g.11758506C=CA1764074474GATA4c.*31C= (n.*31C=)
n.805C=
c.1357C= (n.1357C=)
8g.11758506C>TCA4630924GATA4c.*31C>T (n.*31C>T)
n.805C>T
c.1357C>T (n.1357C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758507G>ACA580031764GATA4c.*32G>A (n.*32G>A)
n.806G>A
c.1358G>A (n.1358G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758507G=CA1764074477GATA4c.*32G= (n.*32G=)
n.806G=
c.1358G= (n.1358G=)
8g.11758508G>CCA4630925GATA4c.*33G>C (n.*33G>C)
n.807G>C
c.1359G>C (n.1359G>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758508G=CA1764074478GATA4c.*33G= (n.*33G=)
n.807G=
c.1359G= (n.1359G=)
8g.11758509A=CA1764074480GATA4c.*34A= (n.*34A=)
n.808A=
c.1360A= (n.1360A=)
8g.11758509A>TCA4630926GATA4c.*34A>T (n.*34A>T)
n.808A>T
c.1360A>T (n.1360A>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758510C>ACA580031765GATA4c.*35C>A (n.*35C>A)
n.809C>A
c.1361C>A (n.1361C>A)
 dbSNP gnomAD v2 gnomAD v4
8g.11758510C=CA1764074482GATA4c.*35C= (n.*35C=)
n.809C=
c.1361C= (n.1361C=)
8g.11758510C>GCA580031766GATA4c.*35C>G (n.*35C>G)
n.809C>G
c.1361C>G (n.1361C>G)
 dbSNP gnomAD v2 gnomAD v4
8g.11758511C>ACA2592761250GATA4c.*36C>A (n.*36C>A)
n.810C>A
c.1362C>A (n.1362C>A)
 dbSNP gnomAD v3 gnomAD v4
8g.11758511C=CA1764074484GATA4c.*36C= (n.*36C=)
n.810C=
c.1362C= (n.1362C=)
8g.11758511C>GCA2686137439GATA4c.*36C>G (n.*36C>G)
n.810C>G
c.1362C>G (n.1362C>G)
 gnomAD v4
8g.11758511C>TCA580031767GATA4c.*36C>T (n.*36C>T)
n.810C>T
c.1362C>T (n.1362C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758512T>ACA2686137442GATA4c.*37T>A (n.*37T>A)
n.811T>A
c.1363T>A (n.1363T>A)
 gnomAD v4
8g.11758513G=CA1764074486GATA4c.*38G= (n.*38G=)
n.812G=
c.1364G= (n.1364G=)
8g.11758513G>TCA172121595GATA4c.*38G>T (n.*38G>T)
n.812G>T
c.1364G>T (n.1364G>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.11758514G>ACA4630927GATA4c.*39G>A (n.*39G>A)
n.813G>A
c.1365G>A (n.1365G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758514G=CA1764074487GATA4c.*39G= (n.*39G=)
n.813G=
c.1365G= (n.1365G=)
8g.11758515G>ACA846164265GATA4c.*40G>A (n.*40G>A)
n.814G>A
c.1366G>A (n.1366G>A)
 dbSNP gnomAD v3 gnomAD v4
8g.11758515G=CA1764074490GATA4c.*40G= (n.*40G=)
n.814G=
c.1366G= (n.1366G=)
8g.11758515G>TCA2686137444GATA4c.*40G>T (n.*40G>T)
n.814G>T
c.1366G>T (n.1366G>T)
 gnomAD v4
8g.11758517C>GCA2686137446GATA4c.*42C>G (n.*42C>G)
n.816C>G
c.1368C>G (n.1368C>G)
 gnomAD v4
8g.11758518T>CCA2686137448GATA4c.*43T>C (n.*43T>C)
n.817T>C
c.1369T>C (n.1369T>C)
 gnomAD v4
8g.11758519T>CCA4630928GATA4c.*44T>C (n.*44T>C)
n.818T>C
c.1370T>C (n.1370T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758519T=CA1764074492GATA4c.*44T= (n.*44T=)
n.818T=
c.1370T= (n.1370T=)
8g.11758520G>ACA2686137452GATA4c.*45G>A (n.*45G>A)
n.819G>A
c.1371G>A (n.1371G>A)
 gnomAD v4
8g.11758521dupCA1110747710GATA4c.*46dup (n.*46dup)
n.820dup
c.1372dup (n.1372dup)
 dbSNP gnomAD v3 gnomAD v4
8g.11758521G>ACA2686137454GATA4c.*46G>A (n.*46G>A)
n.820G>A
c.1372G>A (n.1372G>A)
 gnomAD v4
8g.11758522A>GCA2579094236GATA4c.*47A>G (n.*47A>G)
n.821A>G
c.1373A>G (n.1373A>G)
8g.11758523G>ACA2579094237GATA4c.*48G>A (n.*48G>A)
n.822G>A
c.1374G>A (n.1374G>A)
8g.11758524G>ACA1764074497GATA4c.*49G>A (n.*49G>A)
n.823G>A
c.1375G>A (n.1375G>A)
 dbSNP
8g.11758524G>CCA4630929GATA4c.*49G>C (n.*49G>C)
n.823G>C
c.1375G>C (n.1375G>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
8g.11758524G=CA1764074495GATA4c.*49G= (n.*49G=)
n.823G=
c.1375G= (n.1375G=)
8g.11758524G>TCA2523785719GATA4c.*49G>T (n.*49G>T)
n.823G>T
c.1375G>T (n.1375G>T)
 gnomAD v4
8g.11758525A=CA1764074501GATA4c.*50A= (n.*50A=)
n.824A=
c.1376A= (n.1376A=)
8g.11758525A>TCA4630930GATA4c.*50A>T (n.*50A>T)
n.824A>T
c.1376A>T (n.1376A>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758526T>CCA579789432GATA4c.*51T>C (n.*51T>C)
n.825T>C
c.1377T>C (n.1377T>C)
 dbSNP gnomAD v2 gnomAD v4
8g.11758526T=CA1764074503GATA4c.*51T= (n.*51T=)
n.825T=
c.1377T= (n.1377T=)
8g.11758527A>GCA2686137458GATA4c.*52A>G (n.*52A>G)
n.826A>G
c.1378A>G (n.1378A>G)
 gnomAD v4

Number of alleles fetched