Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.67711404C>A | CA516970160 | AR | c.*236C>A (n.*236C>A) c.1888C>A (p.Arg630=) c.515C>A (n.515C>A) c.292C>A (p.Arg98=) c.1318C>A (p.Arg440=) | dbSNP gnomAD v4 |
X | g.67711404C>T | CA413422950 | AR | c.*236C>T (n.*236C>T) c.1888C>T (p.Arg630Trp) c.515C>T (n.515C>T) c.292C>T (p.Arg98Trp) c.1318C>T (p.Arg440Trp) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |