Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.148741901G>T | CA354889398 | AGTR1 | c.866G>T (p.Cys289Phe) c.953G>T (p.Cys318Phe) c.971G>T (p.Cys324Phe) | ClinVar dbSNP gnomAD v4 |
3 | g.148741901G>A | CA2657402 | AGTR1 | c.866G>A (p.Cys289Tyr) c.953G>A (p.Cys318Tyr) c.971G>A (p.Cys324Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.148741901G= | CA1409910281 | AGTR1 | c.866G= (p.Cys289=) c.953G= (p.Cys318=) c.971G= (p.Cys324=) | dbSNP |