Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112450352A>T | CA297070 | PTPN11 | c.172A>T (p.Asn58Tyr) c.169A>T (p.Asn57Tyr) | ClinVar dbSNP COSMIC |
12 | g.112450352A>G | CA261558 | PTPN11 | c.172A>G (p.Asn58Asp) c.169A>G (p.Asn57Asp) | ClinVar dbSNP |
12 | g.112450352A>C | CA235310 | PTPN11 | c.172A>C (p.Asn58His) c.169A>C (p.Asn57His) | ClinVar dbSNP |