| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67717562G>T | CA16608903 | AR | c.*606G>T (n.*606G>T) c.2258G>T (p.Arg753Leu) c.885G>T (n.885G>T) c.2173+5873G>T (n.2173+5873G>T) c.662G>T (p.Arg221Leu) c.1688G>T (p.Arg563Leu) | ClinVar dbSNP |
| X | g.67717562G>C | CA413424671 | AR | c.*606G>C (n.*606G>C) c.2258G>C (p.Arg753Pro) c.885G>C (n.885G>C) c.2173+5873G>C (n.2173+5873G>C) c.662G>C (p.Arg221Pro) c.1688G>C (p.Arg563Pro) | dbSNP |
| X | g.67717562G>A | CA413424670 | AR | c.*606G>A (n.*606G>A) c.2258G>A (p.Arg753Gln) c.885G>A (n.885G>A) c.2173+5873G>A (n.2173+5873G>A) c.662G>A (p.Arg221Gln) c.1688G>A (p.Arg563Gln) | ClinVar dbSNP COSMIC COSMIC COSMIC |