Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112450361G>C | CA282070 | PTPN11 | c.181G>C (p.Asp61His) c.178G>C (p.Asp60His) | ClinVar dbSNP COSMIC |
12 | g.112450361G>A | CA235316 | PTPN11 | c.181G>A (p.Asp61Asn) c.178G>A (p.Asp60Asn) | ClinVar dbSNP gnomAD v4 COSMIC |
12 | g.112450361G>T | CA10576907 | PTPN11 | c.181G>T (p.Asp61Tyr) c.178G>T (p.Asp60Tyr) | ClinVar dbSNP COSMIC |