Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.101504430A>G | CA10581551 | TRPC6 | c.539T>C (p.Ile180Thr) c.374T>C (p.Ile125Thr) n.895T>C | ClinVar dbSNP |
11 | g.101504430A>T | CA382450126 | TRPC6 | c.539T>A (p.Ile180Asn) c.374T>A (p.Ile125Asn) n.895T>A | dbSNP gnomAD v2 gnomAD v4 |