| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.112450359G>T | CA284662 | PTPN11 | c.179G>T (p.Gly60Val) c.176G>T (p.Gly59Val) | ClinVar dbSNP COSMIC |
| 12 | g.112450359G>C | CA261562 | PTPN11 | c.179G>C (p.Gly60Ala) c.176G>C (p.Gly59Ala) | ClinVar dbSNP gnomAD v4 COSMIC |
| 12 | g.112450359G>A | CA386777568 | PTPN11 | c.179G>A (p.Gly60Asp) c.176G>A (p.Gly59Asp) | ClinVar dbSNP gnomAD v4 |