| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.101504514A>G | CA10581552 | TRPC6 | c.455T>C (p.Leu152Pro) c.290T>C (p.Leu97Pro) n.811T>C | ClinVar dbSNP gnomAD v4 |
| 11 | g.101504514A= | CA1995874918 | TRPC6 | c.455T= (p.Leu152=) c.290T= (p.Leu97=) n.811T= | dbSNP |