Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.17387319T>A | CA379770851 | KCNJ11 | c.512A>T (p.Tyr171Phe) c.773A>T (p.Tyr258Phe) n.931A>T | |
11 | g.17387319T>C | CA5902249 | KCNJ11 | c.512A>G (p.Tyr171Cys) c.773A>G (p.Tyr258Cys) n.931A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.17387319T>G | CA379770855 | KCNJ11 | c.512A>C (p.Tyr171Ser) c.773A>C (p.Tyr258Ser) n.931A>C | |
11 | g.17387319T= | CA1955119211 | KCNJ11 | c.512A= (p.Tyr171=) c.773A= (p.Tyr258=) n.931A= | |
11 | g.17387320A= | CA1955119212 | KCNJ11 | c.511T= (p.Tyr171=) c.772T= (p.Tyr258=) n.930T= | |
11 | g.17387320A>C | CA379770859 | KCNJ11 | c.511T>G (p.Tyr171Asp) c.772T>G (p.Tyr258Asp) n.930T>G | |
11 | g.17387320A>G | CA5902250 | KCNJ11 | c.511T>C (p.Tyr171His) c.772T>C (p.Tyr258His) n.930T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.17387320A>T | CA379770868 | KCNJ11 | c.511T>A (p.Tyr171Asn) c.772T>A (p.Tyr258Asn) n.930T>A | |
11 | g.17387320dup | CA912971887 | KCNJ11 | c.511dup (p.Tyr171LeufsTer5) c.772dup (p.Tyr258LeufsTer5) n.930dup | |
11 | g.17387321G>A | CA473515431 | KCNJ11 | c.510C>T (p.Ile170=) c.771C>T (p.Ile257=) n.929C>T | |
11 | g.17387321G>C | CA379770871 | KCNJ11 | c.510C>G (p.Ile170Met) c.771C>G (p.Ile257Met) n.929C>G | gnomAD v4 |
11 | g.17387321G>T | CA473515434 | KCNJ11 | c.510C>A (p.Ile170=) c.771C>A (p.Ile257=) n.929C>A | |
11 | g.17387321_17387327dup | CA658822453 | KCNJ11 | c.504_510dup (p.Tyr171AspfsTer7) c.765_771dup (p.Tyr258AspfsTer7) n.923_929dup | ClinVar dbSNP |
11 | g.17387322A>C | CA379770877 | KCNJ11 | c.509T>G (p.Ile170Ser) c.770T>G (p.Ile257Ser) n.928T>G | |
11 | g.17387322A>G | CA379770882 | KCNJ11 | c.509T>C (p.Ile170Thr) c.770T>C (p.Ile257Thr) n.928T>C | |
11 | g.17387322A>T | CA379770881 | KCNJ11 | c.509T>A (p.Ile170Asn) c.770T>A (p.Ile257Asn) n.928T>A | |
11 | g.17387323T>A | CA379770887 | KCNJ11 | c.508A>T (p.Ile170Phe) c.769A>T (p.Ile257Phe) n.927A>T | |
11 | g.17387323T>C | CA379770893 | KCNJ11 | c.508A>G (p.Ile170Val) c.769A>G (p.Ile257Val) n.927A>G | gnomAD v4 |
11 | g.17387323T>G | CA379770889 | KCNJ11 | c.508A>C (p.Ile170Leu) c.769A>C (p.Ile257Leu) n.927A>C | |
11 | g.17387324G>A | CA473515435 | KCNJ11 | c.507C>T (p.Ile169=) c.768C>T (p.Ile256=) n.926C>T | dbSNP |
11 | g.17387324G>C | CA379770896 | KCNJ11 | c.507C>G (p.Ile169Met) c.768C>G (p.Ile256Met) n.926C>G | |
11 | g.17387324G= | CA1955119213 | KCNJ11 | c.507C= (p.Ile169=) c.768C= (p.Ile256=) n.926C= | |
11 | g.17387324G>T | CA473515438 | KCNJ11 | c.507C>A (p.Ile169=) c.768C>A (p.Ile256=) n.926C>A | |
11 | g.17387325A>C | CA379770900 | KCNJ11 | c.506T>G (p.Ile169Ser) c.767T>G (p.Ile256Ser) n.925T>G | |
11 | g.17387325A>G | CA379770902 | KCNJ11 | c.506T>C (p.Ile169Thr) c.767T>C (p.Ile256Thr) n.925T>C | |
11 | g.17387325A>T | CA379770904 | KCNJ11 | c.506T>A (p.Ile169Asn) c.767T>A (p.Ile256Asn) n.925T>A | |
11 | g.17387326T>A | CA379770909 | KCNJ11 | c.505A>T (p.Ile169Phe) c.766A>T (p.Ile256Phe) n.924A>T | |
11 | g.17387326T>C | CA379770911 | KCNJ11 | c.505A>G (p.Ile169Val) c.766A>G (p.Ile256Val) n.924A>G | |
11 | g.17387326T>G | CA379770914 | KCNJ11 | c.505A>C (p.Ile169Leu) c.766A>C (p.Ile256Leu) n.924A>C | |
11 | g.17387327C>A | CA473515440 | KCNJ11 | c.504G>T (p.Leu168=) c.765G>T (p.Leu255=) n.923G>T | dbSNP |
11 | g.17387327C= | CA1955119214 | KCNJ11 | c.504G= (p.Leu168=) c.765G= (p.Leu255=) n.923G= | |
11 | g.17387327C>G | CA473515441 | KCNJ11 | c.504G>C (p.Leu168=) c.765G>C (p.Leu255=) n.923G>C | |
11 | g.17387327C>T | CA473515442 | KCNJ11 | c.504G>A (p.Leu168=) c.765G>A (p.Leu255=) n.923G>A | dbSNP gnomAD v2 |
11 | g.17387328A>C | CA379770917 | KCNJ11 | c.503T>G (p.Leu168Arg) c.764T>G (p.Leu255Arg) n.922T>G | |
11 | g.17387328A>G | CA379770920 | KCNJ11 | c.503T>C (p.Leu168Pro) c.764T>C (p.Leu255Pro) n.922T>C | |
11 | g.17387328A>T | CA379770923 | KCNJ11 | c.503T>A (p.Leu168Gln) c.764T>A (p.Leu255Gln) n.922T>A | |
11 | g.17387329G>A | CA473515443 | KCNJ11 | c.502C>T (p.Leu168=) c.763C>T (p.Leu255=) n.921C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.17387329G>C | CA379770924 | KCNJ11 | c.502C>G (p.Leu168Val) c.763C>G (p.Leu255Val) n.921C>G | |
11 | g.17387329G= | CA1955119215 | KCNJ11 | c.502C= (p.Leu168=) c.763C= (p.Leu255=) n.921C= | |
11 | g.17387329G>T | CA379770927 | KCNJ11 | c.502C>A (p.Leu168Met) c.763C>A (p.Leu255Met) n.921C>A | |
11 | g.17387330C>A | CA473515444 | KCNJ11 | c.501G>T (p.Pro167=) c.762G>T (p.Pro254=) n.920G>T | |
11 | g.17387330C= | CA1955119216 | KCNJ11 | c.501G= (p.Pro167=) c.762G= (p.Pro254=) n.920G= | |
11 | g.17387330C>G | CA473515445 | KCNJ11 | c.501G>C (p.Pro167=) c.762G>C (p.Pro254=) n.920G>C | |
11 | g.17387330C>T | CA5902251 | KCNJ11 | c.501G>A (p.Pro167=) c.762G>A (p.Pro254=) n.920G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.17387331G>A | CA254520 | KCNJ11 | c.500C>T (p.Pro167Leu) c.761C>T (p.Pro254Leu) n.919C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.17387331G>C | CA379770937 | KCNJ11 | c.500C>G (p.Pro167Arg) c.761C>G (p.Pro254Arg) n.919C>G | |
11 | g.17387331G= | CA1955119217 | KCNJ11 | c.500C= (p.Pro167=) c.761C= (p.Pro254=) n.919C= | |
11 | g.17387331G>T | CA379770938 | KCNJ11 | c.500C>A (p.Pro167Gln) c.761C>A (p.Pro254Gln) n.919C>A | |
11 | g.17387332G>A | CA379770942 | KCNJ11 | c.499C>T (p.Pro167Ser) c.760C>T (p.Pro254Ser) n.918C>T | gnomAD v4 |
11 | g.17387332G>C | CA379770944 | KCNJ11 | c.499C>G (p.Pro167Ala) c.760C>G (p.Pro254Ala) n.918C>G |