| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.74074779dup | CA261764 | VCL | c.659dup (p.Asn220LysfsTer21) n.332-26275dup n.617dup c.*414dup (n.*414dup) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.74074778_74074779del | CA1139661512 | VCL | c.658_659del (p.Asn220ProfsTer20) n.332-26276_332-26275del n.616_617del c.*413_*414del (n.*413_*414del) | ClinVar dbSNP |