| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48981590G>T | CA143728 | WNT1 | c.1063G>T (p.Val355Phe) c.1030G>T (p.Val344Phe) | ClinVar dbSNP gnomAD v4 |
| 12 | g.48981590G>C | CA384639074 | WNT1 | c.1063G>C (p.Val355Leu) c.1030G>C (p.Val344Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48981590G= | CA2034902105 | WNT1 | c.1063G= (p.Val355=) c.1030G= (p.Val344=) | dbSNP |