Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.48980630G>A | CA236608583 | WNT1 | c.565G>A (p.Glu189Lys) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.48980630G>T | CA143723 | WNT1 | c.565G>T (p.Glu189Ter) | ClinVar dbSNP gnomAD v4 |
12 | g.48980630G= | CA2034925339 | WNT1 | c.565G= (p.Glu189=) | dbSNP |
12 | g.48980630G>C | CA384632232 | WNT1 | c.565G>C (p.Glu189Gln) | dbSNP gnomAD v4 |