Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.66850398G>A | CA341765 | PC | c.2540C>T (p.Ala847Val) n.290-333C>T c.*549C>T (n.*549C>T) c.*1016C>T (n.*1016C>T) c.1019C>T (p.Ala340Val) c.1244C>T (p.Ala415Val) c.1175C>T (p.Ala392Val) | dbSNP |
11 | g.66850398G>C | CA381492744 | PC | c.2540C>G (p.Ala847Gly) n.290-333C>G c.*549C>G (n.*549C>G) c.*1016C>G (n.*1016C>G) c.1019C>G (p.Ala340Gly) c.1244C>G (p.Ala415Gly) c.1175C>G (p.Ala392Gly) | dbSNP |
11 | g.66850398G= | CA1979879554 | PC | c.2540C= (p.Ala847=) n.290-333C= c.*549C= (n.*549C=) c.*1016C= (n.*1016C=) c.1019C= (p.Ala340=) c.1244C= (p.Ala415=) c.1175C= (p.Ala392=) | dbSNP |