Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2583448_2583450delCA891843060KCNQ1c.935_937del (p.Thr312del)
c.554_556del (p.Thr185del)
ClinVar
11g.2583445C>ACA379132964KCNQ1c.932C>A (p.Thr311Asn)
c.551C>A (p.Thr184Asn)
11g.2583445C>GCA379132965KCNQ1c.932C>G (p.Thr311Ser)
c.551C>G (p.Thr184Ser)
11g.2583445C>TCA008752KCNQ1c.932C>T (p.Thr311Ile)
c.551C>T (p.Thr184Ile)
ClinVar dbSNP gnomAD
11g.2583446C>ACA472038401KCNQ1c.933C>A (p.Thr311=)
c.552C>A (p.Thr184=)
COSMIC COSMIC
11g.2583446C>GCA472038402KCNQ1c.933C>G (p.Thr311=)
c.552C>G (p.Thr184=)
11g.2583446C>TCA472038403KCNQ1c.933C>T (p.Thr311=)
c.552C>T (p.Thr184=)
11g.2583447delCA645569428KCNQ1c.934del (p.Thr312ProfsTer?)
c.553del (p.Thr185ProfsTer?)
COSMIC COSMIC
11g.2583447A>CCA379132968KCNQ1c.934A>C (p.Thr312Pro)
c.553A>C (p.Thr185Pro)
11g.2583447A>GCA379132967KCNQ1c.934A>G (p.Thr312Ala)
c.553A>G (p.Thr185Ala)
11g.2583447A>TCA379132966KCNQ1c.934A>T (p.Thr312Ser)
c.553A>T (p.Thr185Ser)
ClinVar
11g.2583448C>ACA379132969KCNQ1c.935C>A (p.Thr312Asn)
c.554C>A (p.Thr185Asn)
11g.2583448C>GCA379132970KCNQ1c.935C>G (p.Thr312Ser)
c.554C>G (p.Thr185Ser)
11g.2583448C>TCA008759KCNQ1c.935C>T (p.Thr312Ile)
c.554C>T (p.Thr185Ile)
ClinVar dbSNP
11g.2583449C>ACA472038404KCNQ1c.936C>A (p.Thr312=)
c.555C>A (p.Thr185=)
11g.2583449C>GCA472038405KCNQ1c.936C>G (p.Thr312=)
c.555C>G (p.Thr185=)
11g.2583449C>TCA041750KCNQ1c.936C>T (p.Thr312=)
c.555C>T (p.Thr185=)
dbSNP ExAC gnomAD
11g.2583450A>CCA379132973KCNQ1c.937A>C (p.Ile313Leu)
c.556A>C (p.Ile186Leu)
11g.2583450A>GCA379132971KCNQ1c.937A>G (p.Ile313Val)
c.556A>G (p.Ile186Val)
11g.2583450A>TCA379132972KCNQ1c.937A>T (p.Ile313Phe)
c.556A>T (p.Ile186Phe)
11g.2583451T>ACA379132974KCNQ1c.938T>A (p.Ile313Asn)
c.557T>A (p.Ile186Asn)
11g.2583451T>CCA379132975KCNQ1c.938T>C (p.Ile313Thr)
c.557T>C (p.Ile186Thr)
11g.2583451T>GCA379132976KCNQ1c.938T>G (p.Ile313Ser)
c.557T>G (p.Ile186Ser)
11g.2583452C>ACA472038406KCNQ1c.939C>A (p.Ile313=)
c.558C>A (p.Ile186=)
11g.2583452C>GCA008767KCNQ1c.939C>G (p.Ile313Met)
c.558C>G (p.Ile186Met)
ClinVar dbSNP
11g.2583452C>TCA041764KCNQ1c.939C>T (p.Ile313=)
c.558C>T (p.Ile186=)
ClinVar dbSNP ExAC gnomAD
11g.2583453G>ACA008773KCNQ1c.940G>A (p.Gly314Ser)
c.559G>A (p.Gly187Ser)
ClinVar dbSNP
11g.2583453G>CCA008777KCNQ1c.940G>C (p.Gly314Arg)
c.559G>C (p.Gly187Arg)
ClinVar dbSNP
11g.2583453G>TCA008786KCNQ1c.940G>T (p.Gly314Cys)
c.559G>T (p.Gly187Cys)
ClinVar dbSNP
11g.2583454G>ACA008793KCNQ1c.941G>A (p.Gly314Asp)
c.560G>A (p.Gly187Asp)
ClinVar dbSNP
11g.2583454G>CCA008798KCNQ1c.941G>C (p.Gly314Ala)
c.560G>C (p.Gly187Ala)
ClinVar dbSNP
11g.2583454G>TCA379132977KCNQ1c.941G>T (p.Gly314Val)
c.560G>T (p.Gly187Val)
11g.2583455C>ACA472038407KCNQ1c.942C>A (p.Gly314=)
c.561C>A (p.Gly187=)
11g.2583455C>GCA472038408KCNQ1c.942C>G (p.Gly314=)
c.561C>G (p.Gly187=)
11g.2583455C>TCA472038409KCNQ1c.942C>T (p.Gly314=)
c.561C>T (p.Gly187=)
11g.2583456T>ACA379132980KCNQ1c.943T>A (p.Tyr315Asn)
c.562T>A (p.Tyr188Asn)
11g.2583456T>CCA379132979KCNQ1c.943T>C (p.Tyr315His)
c.562T>C (p.Tyr188His)
ClinVar
11g.2583456T>GCA379132978KCNQ1c.943T>G (p.Tyr315Asp)
c.562T>G (p.Tyr188Asp)
11g.2583457A>CCA008803KCNQ1c.944A>C (p.Tyr315Ser)
c.563A>C (p.Tyr188Ser)
ClinVar dbSNP
11g.2583457A>GCA008807KCNQ1c.944A>G (p.Tyr315Cys)
c.563A>G (p.Tyr188Cys)
ClinVar dbSNP COSMIC
11g.2583457A>TCA008817KCNQ1c.944A>T (p.Tyr315Phe)
c.563A>T (p.Tyr188Phe)
ClinVar dbSNP COSMIC
11g.2583458T>ACA379132981KCNQ1c.945T>A (p.Tyr315Ter)
c.564T>A (p.Tyr188Ter)
11g.2583458T>CCA041785KCNQ1c.945T>C (p.Tyr315=)
c.564T>C (p.Tyr188=)
dbSNP ExAC gnomAD
11g.2583458T>GCA379132982KCNQ1c.945T>G (p.Tyr315Ter)
c.564T>G (p.Tyr188Ter)
11g.2583459G>ACA008823KCNQ1c.946G>A (p.Gly316Arg)
c.565G>A (p.Gly189Arg)
ClinVar dbSNP
11g.2583459G>CCA008832KCNQ1c.946G>C (p.Gly316Arg)
c.565G>C (p.Gly189Arg)
ClinVar dbSNP
11g.2583459G>TCA008840KCNQ1c.946G>T (p.Gly316Trp)
c.565G>T (p.Gly189Trp)
ClinVar dbSNP
11g.2583460G>ACA008848KCNQ1c.947G>A (p.Gly316Glu)
c.566G>A (p.Gly189Glu)
ClinVar dbSNP
11g.2583460G>CCA379132983KCNQ1c.947G>C (p.Gly316Ala)
c.566G>C (p.Gly189Ala)
11g.2583460G>TCA008856KCNQ1c.947G>T (p.Gly316Val)
c.566G>T (p.Gly189Val)
ClinVar dbSNP

Number of alleles fetched