| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723711C>G | CA120743 | AR | c.*981C>G (n.*981C>G) c.2633C>G (p.Thr878Ser) c.1260C>G (n.1260C>G) c.2199C>G (p.His733Gln) c.1037C>G (p.Thr346Ser) c.2084C>G (p.Thr695Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC |
| X | g.67723711C>T | CA413428204 | AR | c.*981C>T (n.*981C>T) c.2633C>T (p.Thr878Ile) c.1260C>T (n.1260C>T) c.2199C>T (p.His733=) c.1037C>T (p.Thr346Ile) c.2084C>T (p.Thr695Ile) | ClinVar dbSNP |
| X | g.67723711C= | CA2435134791 | AR | c.*981C= (n.*981C=) c.2633C= (p.Thr878=) c.1260C= (n.1260C=) c.2199C= (p.His733=) c.1037C= (p.Thr346=) c.2084C= (p.Thr695=) | dbSNP |