Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.127854354A>G | CA257569 | ENG | c.2T>C (p.Met1Thr) | ClinVar dbSNP |
9 | g.127854354A>C | CA374989708 | ENG | c.2T>G (p.Met1Arg) | ClinVar dbSNP |
9 | g.127854354A>T | CA374989710 | ENG | c.2T>A (p.Met1Lys) | dbSNP gnomAD v4 |
9 | g.127854354A= | CA1879998828 | ENG | c.2T= (p.Met1=) | dbSNP |