Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112450358G>A | CA235370 | PTPN11 | c.178G>A (p.Gly60Ser) c.175G>A (p.Gly59Ser) | ClinVar dbSNP gnomAD v4 |
12 | g.112450358G>T | CA215448 | PTPN11 | c.178G>T (p.Gly60Cys) c.175G>T (p.Gly59Cys) | ClinVar dbSNP |
12 | g.112450358G>C | CA16042862 | PTPN11 | c.178G>C (p.Gly60Arg) c.175G>C (p.Gly59Arg) | ClinVar dbSNP COSMIC |