Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.41114115A>G | CA083614 | PLCG1-AS1,TOP1 | c.1598A>G (p.Asp533Gly) c.191A>G (p.Asp64Gly) n.6384A>G c.*1293A>G (n.*1293A>G) n.2906A>G n.2860A>G n.711-12826T>C c.1094A>G (p.Asp365Gly) c.860A>G (p.Asp287Gly) | ClinVar dbSNP |
20 | g.41114115A= | CA2364229954 | PLCG1-AS1,TOP1 | c.1598A= (p.Asp533=) c.191A= (p.Asp64=) n.6384A= c.*1293A= (n.*1293A=) n.2906A= n.2860A= n.711-12826T= c.1094A= (p.Asp365=) c.860A= (p.Asp287=) | dbSNP |