Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.101472320A>G | CA10581535 | TRPC6 | c.2022T>C (p.Ser674=) c.1674T>C (p.Ser558=) c.1857T>C (p.Ser619=) c.1788T>C (p.Ser596=) n.2378T>C | ClinVar dbSNP |
11 | g.101472320A= | CA1995899027 | TRPC6 | c.2022T= (p.Ser674=) c.1674T= (p.Ser558=) c.1857T= (p.Ser619=) c.1788T= (p.Ser596=) n.2378T= | dbSNP |