| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.37403359C>A | CA408932594 | SRC | c.1642C>A (p.Gln548Lys) c.1591C>A (p.Gln531Lys) c.1609C>A (p.Gln537Lys) n.1237C>A | dbSNP gnomAD v4 |
| 20 | g.37403359C>T | CA122517 | SRC | c.1642C>T (p.Gln548Ter) c.1591C>T (p.Gln531Ter) c.1609C>T (p.Gln537Ter) n.1237C>T | ClinVar dbSNP gnomAD v4 COSMIC |