| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36265860A>G | CA353702 | APOL1 | c.1024A>G (p.Ser342Gly) c.*786A>G (n.*786A>G) c.1111A>G (p.Ser371Gly) c.1072A>G (p.Ser358Gly) c.970A>G (p.Ser324Gly) c.661A>G (p.Ser221Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.36265860A= | CA2403786942 | APOL1 | c.1024A= (p.Ser342=) c.*786A= (n.*786A=) c.1111A= (p.Ser371=) c.1072A= (p.Ser358=) c.970A= (p.Ser324=) c.661A= (p.Ser221=) | dbSNP |