Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.65545379T>C | CA14384066 | AXIN2 | c.957-3822A>G (n.957-3822A>G) c.1272-3822A>G c.396+12846A>G (n.396+12846A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.65545379T>A | CA2270888257 | AXIN2 | c.957-3822A>T (n.957-3822A>T) c.1272-3822A>T c.396+12846A>T (n.396+12846A>T) | dbSNP |