| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67721876A>G | CA120706 | AR | c.*710A>G (n.*710A>G) c.2362A>G (p.Met788Val) c.989A>G (n.989A>G) c.2174-1810A>G (n.2174-1810A>G) c.766A>G (p.Met256Val) c.1792A>G (p.Met598Val) | ClinVar dbSNP |
| X | g.67721876A>T | CA413426595 | AR | c.*710A>T (n.*710A>T) c.2362A>T (p.Met788Leu) c.989A>T (n.989A>T) c.2174-1810A>T (n.2174-1810A>T) c.766A>T (p.Met256Leu) c.1792A>T (p.Met598Leu) | dbSNP |