Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.101469451T>C | CA10581531 | TRPC6 | c.2460A>G (p.Ser820=) c.2112A>G (p.Ser704=) c.2295A>G (p.Ser765=) c.2226A>G (p.Ser742=) c.2409+1732A>G (n.2409+1732A>G) n.2816A>G | ClinVar dbSNP |
11 | g.101469451T= | CA1995897707 | TRPC6 | c.2460A= (p.Ser820=) c.2112A= (p.Ser704=) c.2295A= (p.Ser765=) c.2226A= (p.Ser742=) c.2409+1732A= (n.2409+1732A=) n.2816A= | dbSNP |