| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.49457751G>C | CA10575877 | MMUT | c.693C>G (p.Tyr231Ter) | ClinVar dbSNP |
| 6 | g.49457751G>A | CA450608766 | MMUT | c.693C>T (p.Tyr231=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.49457751G= | CA1627392089 | MMUT | c.693C= (p.Tyr231=) | dbSNP |