Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.80055996C>G | CA357473301 | ANTXR2 | c.314G>C (p.Gly105Ala) c.83G>C (p.Gly28Ala) n.266G>C | dbSNP gnomAD v3 gnomAD v4 |
4 | g.80055996C>A | CA357473300 | ANTXR2 | c.314G>T (p.Gly105Val) c.83G>T (p.Gly28Val) n.266G>T | dbSNP gnomAD v4 |
4 | g.80055996C>T | CA252345 | ANTXR2 | c.314G>A (p.Gly105Asp) c.83G>A (p.Gly28Asp) n.266G>A | ClinVar dbSNP gnomAD v4 |