| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.49451521C>T | CA10575866 | MMUT | c.1277G>A (p.Gly426Glu) | ClinVar dbSNP |
| 6 | g.49451521C>G | CA138796331 | MMUT | c.1277G>C (p.Gly426Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.49451521C>A | CA364398742 | MMUT | c.1277G>T (p.Gly426Val) | dbSNP gnomAD v4 |
| 6 | g.49451521C= | CA1627389304 | MMUT | c.1277G= (p.Gly426=) | dbSNP |