Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.125317548G>ACA3071923FAT4c.1137G>A (p.Leu379=)
c.-55+1571G>A (n.-55+1571G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317548G>CCA441366599FAT4c.1137G>C (p.Leu379=)
c.-55+1571G>C (n.-55+1571G>C)
gnomAD v4
4g.125317548G=CA1491600115FAT4c.1137G= (p.Leu379=)
c.-55+1571G= (n.-55+1571G=)
4g.125317548G>TCA441366600FAT4c.1137G>T (p.Leu379=)
c.-55+1571G>T (n.-55+1571G>T)
4g.125317549C>ACA358117278FAT4c.1138C>A (p.Leu380Ile)
c.-55+1572C>A (n.-55+1572C>A)
4g.125317549C>GCA358117277FAT4c.1138C>G (p.Leu380Val)
c.-55+1572C>G (n.-55+1572C>G)
4g.125317549C>TCA358117279FAT4c.1138C>T (p.Leu380Phe)
c.-55+1572C>T (n.-55+1572C>T)
gnomAD v4
4g.125317550T>ACA358117280FAT4c.1139T>A (p.Leu380His)
c.-55+1573T>A (n.-55+1573T>A)
4g.125317550T>CCA358117281FAT4c.1139T>C (p.Leu380Pro)
c.-55+1573T>C (n.-55+1573T>C)
4g.125317550T>GCA358117282FAT4c.1139T>G (p.Leu380Arg)
c.-55+1573T>G (n.-55+1573T>G)
4g.125317551C>ACA441366606FAT4c.1140C>A (p.Leu380=)
c.-55+1574C>A (n.-55+1574C>A)
gnomAD v4
4g.125317551C>GCA441366605FAT4c.1140C>G (p.Leu380=)
c.-55+1574C>G (n.-55+1574C>G)
4g.125317551C>TCA441366604FAT4c.1140C>T (p.Leu380=)
c.-55+1574C>T (n.-55+1574C>T)
gnomAD v4
4g.125317552A>CCA358117283FAT4c.1141A>C (p.Thr381Pro)
c.-55+1575A>C (n.-55+1575A>C)
4g.125317552A>GCA358117284FAT4c.1141A>G (p.Thr381Ala)
c.-55+1575A>G (n.-55+1575A>G)
4g.125317552A>TCA358117285FAT4c.1141A>T (p.Thr381Ser)
c.-55+1575A>T (n.-55+1575A>T)
4g.125317553C>ACA358117286FAT4c.1142C>A (p.Thr381Asn)
c.-55+1576C>A (n.-55+1576C>A)
4g.125317553C>GCA358117287FAT4c.1142C>G (p.Thr381Ser)
c.-55+1576C>G (n.-55+1576C>G)
4g.125317553C>TCA358117288FAT4c.1142C>T (p.Thr381Ile)
c.-55+1576C>T (n.-55+1576C>T)
4g.125317554C>ACA441366611FAT4c.1143C>A (p.Thr381=)
c.-55+1577C>A (n.-55+1577C>A)
4g.125317554C=CA1491600118FAT4c.1143C= (p.Thr381=)
c.-55+1577C= (n.-55+1577C=)
4g.125317554C>GCA441366613FAT4c.1143C>G (p.Thr381=)
c.-55+1577C>G (n.-55+1577C>G)
4g.125317554C>TCA104861873FAT4c.1143C>T (p.Thr381=)
c.-55+1577C>T (n.-55+1577C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.125317555G>ACA3071924FAT4c.1144G>A (p.Val382Met)
c.-55+1578G>A (n.-55+1578G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317555G>CCA358117289FAT4c.1144G>C (p.Val382Leu)
c.-55+1578G>C (n.-55+1578G>C)
4g.125317555G=CA1491600122FAT4c.1144G= (p.Val382=)
c.-55+1578G= (n.-55+1578G=)
4g.125317555G>TCA358117290FAT4c.1144G>T (p.Val382Leu)
c.-55+1578G>T (n.-55+1578G>T)
4g.125317556T>ACA358117291FAT4c.1145T>A (p.Val382Glu)
c.-55+1579T>A (n.-55+1579T>A)
4g.125317556T>CCA358117293FAT4c.1145T>C (p.Val382Ala)
c.-55+1579T>C (n.-55+1579T>C)
4g.125317556T>GCA358117292FAT4c.1145T>G (p.Val382Gly)
c.-55+1579T>G (n.-55+1579T>G)
4g.125317557G>ACA441366619FAT4c.1146G>A (p.Val382=)
c.-55+1580G>A (n.-55+1580G>A)
gnomAD v4
4g.125317557G>CCA441366620FAT4c.1146G>C (p.Val382=)
c.-55+1580G>C (n.-55+1580G>C)
4g.125317557G>TCA441366621FAT4c.1146G>T (p.Val382=)
c.-55+1580G>T (n.-55+1580G>T)
4g.125317558A>CCA358117294FAT4c.1147A>C (p.Thr383Pro)
c.-55+1581A>C (n.-55+1581A>C)
4g.125317558A>GCA358117295FAT4c.1147A>G (p.Thr383Ala)
c.-55+1581A>G (n.-55+1581A>G)
4g.125317558A>TCA358117296FAT4c.1147A>T (p.Thr383Ser)
c.-55+1581A>T (n.-55+1581A>T)
4g.125317559C>ACA358117297FAT4c.1148C>A (p.Thr383Lys)
c.-55+1582C>A (n.-55+1582C>A)
ClinVar gnomAD v4
4g.125317559C>GCA358117298FAT4c.1148C>G (p.Thr383Arg)
c.-55+1582C>G (n.-55+1582C>G)
4g.125317559C>TCA358117299FAT4c.1148C>T (p.Thr383Met)
c.-55+1582C>T (n.-55+1582C>T)
ClinVar gnomAD v4
4g.125317560G>ACA3071925FAT4c.1149G>A (p.Thr383=)
c.-55+1583G>A (n.-55+1583G>A)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
4g.125317560G>CCA441366625FAT4c.1149G>C (p.Thr383=)
c.-55+1583G>C (n.-55+1583G>C)
gnomAD v4
4g.125317560G=CA1491600130FAT4c.1149G= (p.Thr383=)
c.-55+1583G= (n.-55+1583G=)
4g.125317560G>TCA441366626FAT4c.1149G>T (p.Thr383=)
c.-55+1583G>T (n.-55+1583G>T)
4g.125317561G>ACA358117300FAT4c.1150G>A (p.Asp384Asn)
c.-55+1584G>A (n.-55+1584G>A)
4g.125317561G>CCA358117301FAT4c.1150G>C (p.Asp384His)
c.-55+1584G>C (n.-55+1584G>C)
4g.125317561G>TCA358117302FAT4c.1150G>T (p.Asp384Tyr)
c.-55+1584G>T (n.-55+1584G>T)
4g.125317562A>CCA358117305FAT4c.1151A>C (p.Asp384Ala)
c.-55+1585A>C (n.-55+1585A>C)
4g.125317562A>GCA358117304FAT4c.1151A>G (p.Asp384Gly)
c.-55+1585A>G (n.-55+1585A>G)
4g.125317562A>TCA358117303FAT4c.1151A>T (p.Asp384Val)
c.-55+1585A>T (n.-55+1585A>T)
4g.125317563C>ACA358117306FAT4c.1152C>A (p.Asp384Glu)
c.-55+1586C>A (n.-55+1586C>A)

Number of alleles fetched