Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.127423087T>G | CA55345119 | PROC | c.316T>G (p.Cys106Gly) c.*122T>G (n.*122T>G) n.491T>G c.499T>G (p.Cys167Gly) c.379T>G (p.Cys127Gly) c.559T>G (p.Cys187Gly) c.471T>G (p.Ala157=) c.400T>G (p.Cys134Gly) c.292T>G (p.Cys98Gly) c.310T>G (p.Cys104Gly) | dbSNP |
2 | g.127423087T= | CA1286881995 | PROC | c.316T= (p.Cys106=) c.*122T= (n.*122T=) n.491T= c.499T= (p.Cys167=) c.379T= (p.Cys127=) c.559T= (p.Cys187=) c.471T= (p.Ala157=) c.400T= (p.Cys134=) c.292T= (p.Cys98=) c.310T= (p.Cys104=) | dbSNP |