Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49453751G>A | CA364401069 | MMUT | c.917C>T (p.Ser306Phe) | ClinVar dbSNP gnomAD v4 |
6 | g.49453751G>T | CA364401067 | MMUT | c.917C>A (p.Ser306Tyr) | ClinVar dbSNP |
6 | g.49453751G= | CA1627390365 | MMUT | c.917C= (p.Ser306=) | dbSNP |