| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48966479C>G | CA384673501 | WNT10B | c.786G>C (p.Trp262Cys) c.*68G>C (n.*68G>C) c.420G>C (p.Trp140Cys) c.*64G>C (n.*64G>C) | dbSNP gnomAD v4 |
| 12 | g.48966479C>T | CA6544101 | WNT10B | c.786G>A (p.Trp262Ter) c.*68G>A (n.*68G>A) c.420G>A (p.Trp140Ter) c.*64G>A (n.*64G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |