| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.101472200C>T | CA6244199 | TRPC6 | c.2142G>A (p.Thr714=) c.1794G>A (p.Thr598=) c.1977G>A (p.Thr659=) c.1908G>A (p.Thr636=) n.2498G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.101472200C>G | CA6244200 | TRPC6 | c.2142G>C (p.Thr714=) c.1794G>C (p.Thr598=) c.1977G>C (p.Thr659=) c.1908G>C (p.Thr636=) n.2498G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.101472200C>A | CA6244198 | TRPC6 | c.2142G>T (p.Thr714=) c.1794G>T (p.Thr598=) c.1977G>T (p.Thr659=) c.1908G>T (p.Thr636=) n.2498G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |