Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.67722881A>T | CA413427775 | AR | c.*852A>T (n.*852A>T) c.2504A>T (p.Tyr835Phe) c.1131A>T (n.1131A>T) c.2174-805A>T (n.2174-805A>T) c.908A>T (p.Tyr303Phe) c.1955A>T (p.Tyr652Phe) | dbSNP |
X | g.67722881A>G | CA16608548 | AR | c.*852A>G (n.*852A>G) c.2504A>G (p.Tyr835Cys) c.1131A>G (n.1131A>G) c.2174-805A>G (n.2174-805A>G) c.908A>G (p.Tyr303Cys) c.1955A>G (p.Tyr652Cys) | ClinVar dbSNP |