| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.34007995C>T | CA151758 | AMACR,C1QTNF3-AMACR | c.25G>A (p.Val9Met) c.690-2096G>A (n.690-2096G>A) n.37G>A n.765-2096G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.34007995C= | CA1538249648 | AMACR,C1QTNF3-AMACR | c.25G= (p.Val9=) c.690-2096G= (n.690-2096G=) n.37G= n.765-2096G= | dbSNP |