Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.128485837G>C | CA354406006 | GATA2 | c.761C>G (p.Pro254Arg) c.1043C>G (p.Pro348Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.128485837G>A | CA128576 | GATA2 | c.761C>T (p.Pro254Leu) c.1043C>T (p.Pro348Leu) | ClinVar dbSNP |
3 | g.128485837G= | CA1400719127 | GATA2 | c.761C= (p.Pro254=) c.1043C= (p.Pro348=) | dbSNP |