| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.74094449G>T | CA279267 | VCL | c.1531G>T (p.Asp511Tyr) c.547G>T (p.Asp183Tyr) n.332-6605G>T n.4334G>T c.*1286G>T (n.*1286G>T) c.1534G>T (p.Asp512Tyr) | ClinVar dbSNP gnomAD v4 |
| 10 | g.74094449G= | CA1919905202 | VCL | c.1531G= (p.Asp511=) c.547G= (p.Asp183=) n.332-6605G= n.4334G= c.*1286G= (n.*1286G=) c.1534G= (p.Asp512=) | dbSNP |