| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67545785G>A | CA10436303 | AR | c.639G>A (p.Glu213=) n.966G>A c.69G>A (p.Glu23=) c.-1145G>A (n.-1145G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.67545785G>T | CA413425323 | AR | c.639G>T (p.Glu213Asp) n.966G>T c.69G>T (p.Glu23Asp) c.-1145G>T (n.-1145G>T) | dbSNP |