Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.11758366C>GCA4630891GATA4c.1220C>G (p.Pro407Arg)
c.1223C>G (p.Pro408Arg)
n.665C>G
c.602C>G (p.Pro201Arg)
c.1217C>G (p.Pro406Arg)
c.476C>G (p.Pro159Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.11758366C>ACA212683GATA4c.1220C>A (p.Pro407Gln)
c.1223C>A (p.Pro408Gln)
n.665C>A
c.602C>A (p.Pro201Gln)
c.1217C>A (p.Pro406Gln)
c.476C>A (p.Pro159Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.11758366C=CA1764074197GATA4c.1220C= (p.Pro407=)
c.1223C= (p.Pro408=)
n.665C=
c.602C= (p.Pro201=)
c.1217C= (p.Pro406=)
c.476C= (p.Pro159=)
dbSNP

Number of alleles fetched