| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.49453692T>C | CA364400752 | MMUT | c.976A>G (p.Arg326Gly) | ClinVar dbSNP gnomAD v4 |
| 6 | g.49453692T>A | CA364400750 | MMUT | c.976A>T (p.Arg326Ter) | ClinVar dbSNP |
| 6 | g.49453692T= | CA1627390342 | MMUT | c.976A= (p.Arg326=) | dbSNP |