| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48966271G>A | CA118933 | WNT10B | c.994C>T (p.Arg332Trp) c.*276C>T (n.*276C>T) c.628C>T (p.Arg210Trp) c.*272C>T (n.*272C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966271G>C | CA6544052 | WNT10B | c.994C>G (p.Arg332Gly) c.*276C>G (n.*276C>G) c.628C>G (p.Arg210Gly) c.*272C>G (n.*272C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966271G>T | CA6544053 | WNT10B | c.994C>A (p.Arg332=) c.*276C>A (n.*276C>A) c.628C>A (p.Arg210=) c.*272C>A (n.*272C>A) | dbSNP ExAC gnomAD v2 |