Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.127854355T>C | CA16612719 | ENG | c.1A>G (p.Met1Val) | ClinVar dbSNP gnomAD v4 |
9 | g.127854355T>G | CA374989714 | ENG | c.1A>C (p.Met1Leu) | ClinVar dbSNP |
9 | g.127854355T= | CA1879998848 | ENG | c.1A= (p.Met1=) | dbSNP |