| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.65537421C>A | CA293098217 | AXIN2 | c.1615G>T (p.Val539Leu) c.397-8721G>T (n.397-8721G>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.65537421C>T | CA289644 | AXIN2 | c.1615G>A (p.Val539Met) c.397-8721G>A (n.397-8721G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.65537421C= | CA2270884053 | AXIN2 | c.1615G= (p.Val539=) c.397-8721G= (n.397-8721G=) | dbSNP |