| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723745C>G | CA413428282 | AR | c.*1015C>G (n.*1015C>G) c.2667C>G (p.Ser889Arg) c.1294C>G (n.1294C>G) c.*28C>G (n.*28C>G) c.1071C>G (p.Ser357Arg) c.2118C>G (p.Ser706Arg) | dbSNP |
| X | g.67723745C>A | CA413428281 | AR | c.*1015C>A (n.*1015C>A) c.2667C>A (p.Ser889Arg) c.1294C>A (n.1294C>A) c.*28C>A (n.*28C>A) c.1071C>A (p.Ser357Arg) c.2118C>A (p.Ser706Arg) | dbSNP |
| X | g.67723745C>T | CA254897 | AR | c.*1015C>T (n.*1015C>T) c.2667C>T (p.Ser889=) c.1294C>T (n.1294C>T) c.*28C>T (n.*28C>T) c.1071C>T (p.Ser357=) c.2118C>T (p.Ser706=) | ClinVar dbSNP COSMIC COSMIC |