| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.74069359G>A | CA160115111 | ELN | c.*659G>A (n.*659G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.74069359G>C | CA10626399 | ELN | c.*659G>C (n.*659G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.74069359G>T | CA160115112 | ELN | c.*659G>T (n.*659G>T) | dbSNP gnomAD v3 gnomAD v4 |