| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723710A>T | CA413428202 | AR | c.*980A>T (n.*980A>T) c.2632A>T (p.Thr878Ser) c.1259A>T (n.1259A>T) c.2198A>T (p.His733Leu) c.1036A>T (p.Thr346Ser) c.2083A>T (p.Thr695Ser) | dbSNP |
| X | g.67723710A>G | CA120737 | AR | c.*980A>G (n.*980A>G) c.2632A>G (p.Thr878Ala) c.1259A>G (n.1259A>G) c.2198A>G (p.His733Arg) c.1036A>G (p.Thr346Ala) c.2083A>G (p.Thr695Ala) | ClinVar dbSNP COSMIC COSMIC COSMIC |