| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.119364694C>T | CA13399295 | USP2 | c.775-4460G>A (n.775-4460G>A) c.46-4460G>A (n.46-4460G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.119364694C>A | CA2003934269 | USP2 | c.775-4460G>T (n.775-4460G>T) c.46-4460G>T (n.46-4460G>T) | dbSNP |