| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.914504C>T | CA359043457 | TRIP13 | c.1060C>T (p.Arg354Ter) | ClinVar dbSNP gnomAD v4 |
| 5 | g.914504C>G | CA112875739 | TRIP13 | c.1060C>G (p.Arg354Gly) | ClinVar dbSNP gnomAD v4 |
| 5 | g.914504C>A | CA112875740 | TRIP13 | c.1060C>A (p.Arg354=) | dbSNP gnomAD v4 |