| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67721838G>T | CA413426376 | AR | c.*672G>T (n.*672G>T) c.2324G>T (p.Arg775Leu) c.951G>T (n.951G>T) c.2174-1848G>T (n.2174-1848G>T) c.728G>T (p.Arg243Leu) c.1754G>T (p.Arg585Leu) | dbSNP |
| X | g.67721838G>C | CA413426374 | AR | c.*672G>C (n.*672G>C) c.2324G>C (p.Arg775Pro) c.951G>C (n.951G>C) c.2174-1848G>C (n.2174-1848G>C) c.728G>C (p.Arg243Pro) c.1754G>C (p.Arg585Pro) | dbSNP |
| X | g.67721838G>A | CA120712 | AR | c.*672G>A (n.*672G>A) c.2324G>A (p.Arg775His) c.951G>A (n.951G>A) c.2174-1848G>A (n.2174-1848G>A) c.728G>A (p.Arg243His) c.1754G>A (p.Arg585His) | ClinVar dbSNP COSMIC COSMIC COSMIC |