Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.66870409A= | CA1979902758 | PC | c.796T= (p.Ser266=) n.290-20344T= c.676T= (p.Ser226=) | |
11 | g.66870409A>C | CA16606005 | PC | c.796T>G (p.Ser266Ala) n.290-20344T>G c.676T>G (p.Ser226Ala) | ClinVar dbSNP gnomAD v4 |
11 | g.66870409A>G | CA6132104 | PC | c.796T>C (p.Ser266Pro) n.290-20344T>C c.676T>C (p.Ser226Pro) | dbSNP ExAC gnomAD v2 |
11 | g.66870409A>T | CA341775 | PC | c.796T>A (p.Ser266Thr) n.290-20344T>A c.676T>A (p.Ser226Thr) | dbSNP |
11 | g.66870410G>A | CA475375971 | PC | c.795C>T (p.Cys265=) n.290-20345C>T c.675C>T (p.Cys225=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.66870410G>C | CA381501436 | PC | c.795C>G (p.Cys265Trp) n.290-20345C>G c.675C>G (p.Cys225Trp) | |
11 | g.66870410G= | CA1979902763 | PC | c.795C= (p.Cys265=) n.290-20345C= c.675C= (p.Cys225=) | |
11 | g.66870410G>T | CA381501438 | PC | c.795C>A (p.Cys265Ter) n.290-20345C>A c.675C>A (p.Cys225Ter) | |
11 | g.66870411C>A | CA381501441 | PC | c.794G>T (p.Cys265Phe) n.290-20346G>T c.674G>T (p.Cys225Phe) | |
11 | g.66870411C>G | CA381501445 | PC | c.794G>C (p.Cys265Ser) n.290-20346G>C c.674G>C (p.Cys225Ser) | gnomAD v4 |
11 | g.66870411C>T | CA381501443 | PC | c.794G>A (p.Cys265Tyr) n.290-20346G>A c.674G>A (p.Cys225Tyr) | |
11 | g.66870412A>C | CA381501448 | PC | c.793T>G (p.Cys265Gly) n.290-20347T>G c.673T>G (p.Cys225Gly) | |
11 | g.66870412A>G | CA381501450 | PC | c.793T>C (p.Cys265Arg) n.290-20347T>C c.673T>C (p.Cys225Arg) | |
11 | g.66870412A>T | CA381501452 | PC | c.793T>A (p.Cys265Ser) n.290-20347T>A c.673T>A (p.Cys225Ser) | |
11 | g.66870413G>A | CA475375972 | PC | c.792C>T (p.Asp264=) n.290-20348C>T c.672C>T (p.Asp224=) | gnomAD v4 |
11 | g.66870413G>C | CA381501455 | PC | c.792C>G (p.Asp264Glu) n.290-20348C>G c.672C>G (p.Asp224Glu) | |
11 | g.66870413G>T | CA381501458 | PC | c.792C>A (p.Asp264Glu) n.290-20348C>A c.672C>A (p.Asp224Glu) | dbSNP |
11 | g.66870414T>A | CA381501461 | PC | c.791A>T (p.Asp264Val) n.290-20349A>T c.671A>T (p.Asp224Val) | |
11 | g.66870414T>C | CA381501462 | PC | c.791A>G (p.Asp264Gly) n.290-20349A>G c.671A>G (p.Asp224Gly) | |
11 | g.66870414T>G | CA381501464 | PC | c.791A>C (p.Asp264Ala) n.290-20349A>C c.671A>C (p.Asp224Ala) | |
11 | g.66870415C>A | CA381501467 | PC | c.790G>T (p.Asp264Tyr) n.290-20350G>T c.670G>T (p.Asp224Tyr) | |
11 | g.66870415C= | CA1979902769 | PC | c.790G= (p.Asp264=) n.290-20350G= c.670G= (p.Asp224=) | |
11 | g.66870415C>G | CA381501469 | PC | c.790G>C (p.Asp264His) n.290-20350G>C c.670G>C (p.Asp224His) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.66870415C>T | CA381501472 | PC | c.790G>A (p.Asp264Asn) n.290-20350G>A c.670G>A (p.Asp224Asn) | |
11 | g.66870416T>A | CA475375973 | PC | c.789A>T (p.Arg263=) n.290-20351A>T c.669A>T (p.Arg223=) | ClinVar dbSNP |
11 | g.66870416T>C | CA475375974 | PC | c.789A>G (p.Arg263=) n.290-20351A>G c.669A>G (p.Arg223=) | |
11 | g.66870416T>G | CA475375975 | PC | c.789A>C (p.Arg263=) n.290-20351A>C c.669A>C (p.Arg223=) | dbSNP gnomAD v4 |
11 | g.66870416T= | CA1979902772 | PC | c.789A= (p.Arg263=) n.290-20351A= c.669A= (p.Arg223=) | |
11 | g.66870417C>A | CA381501474 | PC | c.788G>T (p.Arg263Leu) n.290-20352G>T c.668G>T (p.Arg223Leu) | |
11 | g.66870417C= | CA1979902791 | PC | c.788G= (p.Arg263=) n.290-20352G= c.668G= (p.Arg223=) | |
11 | g.66870417C>G | CA381501477 | PC | c.788G>C (p.Arg263Pro) n.290-20352G>C c.668G>C (p.Arg223Pro) | |
11 | g.66870417C>T | CA312921 | PC | c.788G>A (p.Arg263Gln) n.290-20352G>A c.668G>A (p.Arg223Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.66870418G>A | CA6132105 | PC | c.787C>T (p.Arg263Ter) n.290-20353C>T c.667C>T (p.Arg223Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.66870418G>C | CA381501481 | PC | c.787C>G (p.Arg263Gly) n.290-20353C>G c.667C>G (p.Arg223Gly) | |
11 | g.66870418G= | CA1979902811 | PC | c.787C= (p.Arg263=) n.290-20353C= c.667C= (p.Arg223=) | |
11 | g.66870418G>T | CA475375976 | PC | c.787C>A (p.Arg263=) n.290-20353C>A c.667C>A (p.Arg223=) | ClinVar |
11 | g.66870419C>A | CA312908 | PC | c.786G>T (p.Glu262Asp) n.290-20354G>T c.666G>T (p.Glu222Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.66870419C= | CA1979902819 | PC | c.786G= (p.Glu262=) n.290-20354G= c.666G= (p.Glu222=) | |
11 | g.66870419C>G | CA381501485 | PC | c.786G>C (p.Glu262Asp) n.290-20354G>C c.666G>C (p.Glu222Asp) | |
11 | g.66870419C>T | CA475375977 | PC | c.786G>A (p.Glu262=) n.290-20354G>A c.666G>A (p.Glu222=) | ClinVar dbSNP gnomAD v4 |
11 | g.66870420T>A | CA381501489 | PC | c.785A>T (p.Glu262Val) n.290-20355A>T c.665A>T (p.Glu222Val) | |
11 | g.66870420T>C | CA381501491 | PC | c.785A>G (p.Glu262Gly) n.290-20355A>G c.665A>G (p.Glu222Gly) | |
11 | g.66870420T>G | CA381501494 | PC | c.785A>C (p.Glu262Ala) n.290-20355A>C c.665A>C (p.Glu222Ala) | |
11 | g.66870421C>A | CA381501503 | PC | c.784G>T (p.Glu262Ter) n.290-20356G>T c.664G>T (p.Glu222Ter) | |
11 | g.66870421C= | CA1979902834 | PC | c.784G= (p.Glu262=) n.290-20356G= c.664G= (p.Glu222=) | |
11 | g.66870421C>G | CA381501500 | PC | c.784G>C (p.Glu262Gln) n.290-20356G>C c.664G>C (p.Glu222Gln) | |
11 | g.66870421C>T | CA381501497 | PC | c.784G>A (p.Glu262Lys) n.290-20356G>A c.664G>A (p.Glu222Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.66870422G>A | CA6132106 | PC | c.783C>T (p.Tyr261=) n.290-20357C>T c.663C>T (p.Tyr221=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.66870422G>C | CA381501507 | PC | c.783C>G (p.Tyr261Ter) n.290-20357C>G c.663C>G (p.Tyr221Ter) | |
11 | g.66870422G= | CA1979902843 | PC | c.783C= (p.Tyr261=) n.290-20357C= c.663C= (p.Tyr221=) |