| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.47857512G>A | CA119030 | VDR | c.454C>T (p.Gln152Ter) c.*456C>T (n.*456C>T) c.604C>T (p.Gln202Ter) c.523C>T (p.Gln175Ter) | ClinVar dbSNP COSMIC COSMIC |
| 12 | g.47857512G= | CA2034414516 | VDR | c.454C= (p.Gln152=) c.*456C= (n.*456C=) c.604C= (p.Gln202=) c.523C= (p.Gln175=) | dbSNP |