Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.11758366C>G | CA4630891 | GATA4 | c.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 |
8 | g.11758366C>A | CA212683 | GATA4 | c.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 |