| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36265520G>A | CA10208734 | APOL1 | c.684G>A (p.Met228Ile) c.*446G>A (n.*446G>A) c.771G>A (p.Met257Ile) c.732G>A (p.Met244Ile) c.630G>A (p.Met210Ile) c.321G>A (p.Met107Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.36265520G>T | CA411366989 | APOL1 | c.684G>T (p.Met228Ile) c.*446G>T (n.*446G>T) c.771G>T (p.Met257Ile) c.732G>T (p.Met244Ile) c.630G>T (p.Met210Ile) c.321G>T (p.Met107Ile) | dbSNP |
| 22 | g.36265520G>C | CA411366988 | APOL1 | c.684G>C (p.Met228Ile) c.*446G>C (n.*446G>C) c.771G>C (p.Met257Ile) c.732G>C (p.Met244Ile) c.630G>C (p.Met210Ile) c.321G>C (p.Met107Ile) | dbSNP gnomAD v2 gnomAD v4 |