| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.112450362A>C | CA273600 | PTPN11 | c.182A>C (p.Asp61Ala) c.179A>C (p.Asp60Ala) | ClinVar dbSNP COSMIC |
| 12 | g.112450362A>T | CA282073 | PTPN11 | c.182A>T (p.Asp61Val) c.179A>T (p.Asp60Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 12 | g.112450362A>G | CA177665 | PTPN11 | c.182A>G (p.Asp61Gly) c.179A>G (p.Asp60Gly) | ClinVar dbSNP gnomAD v4 COSMIC |