| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723701C>A | CA413428177 | AR | c.*971C>A (n.*971C>A) c.2623C>A (p.His875Asn) c.1250C>A (n.1250C>A) c.2189C>A (p.Ala730Glu) c.1027C>A (p.His343Asn) c.2074C>A (p.His692Asn) | dbSNP |
| X | g.67723701C>G | CA413428176 | AR | c.*971C>G (n.*971C>G) c.2623C>G (p.His875Asp) c.1250C>G (n.1250C>G) c.2189C>G (p.Ala730Gly) c.1027C>G (p.His343Asp) c.2074C>G (p.His692Asp) | dbSNP |
| X | g.67723701C>T | CA120746 | AR | c.*971C>T (n.*971C>T) c.2623C>T (p.His875Tyr) c.1250C>T (n.1250C>T) c.2189C>T (p.Ala730Val) c.1027C>T (p.His343Tyr) c.2074C>T (p.His692Tyr) | ClinVar dbSNP COSMIC COSMIC COSMIC |