Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2572870_2572884delCA2695213155KCNQ1c.544_558del (p.Gly182_Leu186del)
c.478-10565_478-10551del (n.478-10565_478-10551del)
c.805_819del (p.Gly269_Leu273del)
c.424_438del (p.Gly142_Leu146del)
c.124-10565_124-10551del (n.124-10565_124-10551del)
11g.2572871G>ACA008292KCNQ1c.545G>A (p.Gly182Asp)
c.478-10564G>A (n.478-10564G>A)
c.806G>A (p.Gly269Asp)
c.425G>A (p.Gly142Asp)
c.124-10564G>A (n.124-10564G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2572871G>CCA379131341KCNQ1c.545G>C (p.Gly182Ala)
c.478-10564G>C (n.478-10564G>C)
c.806G>C (p.Gly269Ala)
c.425G>C (p.Gly142Ala)
c.124-10564G>C (n.124-10564G>C)
11g.2572871G=CA1948243181KCNQ1c.545G= (p.Gly182=)
c.478-10564G= (n.478-10564G=)
c.806G= (p.Gly269=)
c.425G= (p.Gly142=)
c.124-10564G= (n.124-10564G=)
11g.2572871G>TCA008303KCNQ1c.545G>T (p.Gly182Val)
c.478-10564G>T (n.478-10564G>T)
c.806G>T (p.Gly269Val)
c.425G>T (p.Gly142Val)
c.124-10564G>T (n.124-10564G>T)
ClinVar dbSNP
11g.2572872C>ACA472038142KCNQ1c.546C>A (p.Gly182=)
c.478-10563C>A (n.478-10563C>A)
c.807C>A (p.Gly269=)
c.426C>A (p.Gly142=)
c.124-10563C>A (n.124-10563C>A)
11g.2572872C=CA1948243182KCNQ1c.546C= (p.Gly182=)
c.478-10563C= (n.478-10563C=)
c.807C= (p.Gly269=)
c.426C= (p.Gly142=)
c.124-10563C= (n.124-10563C=)
11g.2572872C>GCA472038140KCNQ1c.546C>G (p.Gly182=)
c.478-10563C>G (n.478-10563C>G)
c.807C>G (p.Gly269=)
c.426C>G (p.Gly142=)
c.124-10563C>G (n.124-10563C>G)
11g.2572872C>TCA472038141KCNQ1c.546C>T (p.Gly182=)
c.478-10563C>T (n.478-10563C>T)
c.807C>T (p.Gly269=)
c.426C>T (p.Gly142=)
c.124-10563C>T (n.124-10563C>T)
dbSNP gnomAD v3 gnomAD v4
11g.2572874_2572877delCA2695213156KCNQ1c.548_551del (p.Phe183TrpfsTer18)
c.478-10561_478-10558del (n.478-10561_478-10558del)
c.809_812del (p.Phe270TrpfsTer18)
c.428_431del (p.Phe143TrpfsTer18)
c.124-10561_124-10558del (n.124-10561_124-10558del)
c.548_551del (p.Phe183TrpfsTer?)
11g.2572873T>ACA379131345KCNQ1c.547T>A (p.Phe183Ile)
c.478-10562T>A (n.478-10562T>A)
c.808T>A (p.Phe270Ile)
c.427T>A (p.Phe143Ile)
c.124-10562T>A (n.124-10562T>A)
11g.2572873T>CCA379131347KCNQ1c.547T>C (p.Phe183Leu)
c.478-10562T>C (n.478-10562T>C)
c.808T>C (p.Phe270Leu)
c.427T>C (p.Phe143Leu)
c.124-10562T>C (n.124-10562T>C)
11g.2572873T>GCA379131349KCNQ1c.547T>G (p.Phe183Val)
c.478-10562T>G (n.478-10562T>G)
c.808T>G (p.Phe270Val)
c.427T>G (p.Phe143Val)
c.124-10562T>G (n.124-10562T>G)
11g.2572874T>ACA379131354KCNQ1c.548T>A (p.Phe183Tyr)
c.478-10561T>A (n.478-10561T>A)
c.809T>A (p.Phe270Tyr)
c.428T>A (p.Phe143Tyr)
c.124-10561T>A (n.124-10561T>A)
11g.2572874T>CCA040791KCNQ1c.548T>C (p.Phe183Ser)
c.478-10561T>C (n.478-10561T>C)
c.809T>C (p.Phe270Ser)
c.428T>C (p.Phe143Ser)
c.124-10561T>C (n.124-10561T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2572874T>GCA379131351KCNQ1c.548T>G (p.Phe183Cys)
c.478-10561T>G (n.478-10561T>G)
c.809T>G (p.Phe270Cys)
c.428T>G (p.Phe143Cys)
c.124-10561T>G (n.124-10561T>G)
11g.2572874T=CA1948243183KCNQ1c.548T= (p.Phe183=)
c.478-10561T= (n.478-10561T=)
c.809T= (p.Phe270=)
c.428T= (p.Phe143=)
c.124-10561T= (n.124-10561T=)
11g.2572874_2572880delinsTCCTGGGCA1948243184KCNQ1c.548_554delinsTCCTGGG (p.Phe183=)
c.478-10561_478-10555delinsTCCTGGG (n.478-10561_478-10555delinsTCCTGGG)
c.809_815delinsTCCTGGG (p.Phe270=)
c.428_434delinsTCCTGGG (p.Phe143=)
c.124-10561_124-10555delinsTCCTGGG (n.124-10561_124-10555delinsTCCTGGG)
11g.2572875C>ACA379131356KCNQ1c.549C>A (p.Phe183Leu)
c.478-10560C>A (n.478-10560C>A)
c.810C>A (p.Phe270Leu)
c.429C>A (p.Phe143Leu)
c.124-10560C>A (n.124-10560C>A)
11g.2572875C>GCA379131358KCNQ1c.549C>G (p.Phe183Leu)
c.478-10560C>G (n.478-10560C>G)
c.810C>G (p.Phe270Leu)
c.429C>G (p.Phe143Leu)
c.124-10560C>G (n.124-10560C>G)
11g.2572875C>TCA472038143KCNQ1c.549C>T (p.Phe183=)
c.478-10560C>T (n.478-10560C>T)
c.810C>T (p.Phe270=)
c.429C>T (p.Phe143=)
c.124-10560C>T (n.124-10560C>T)
COSMIC COSMIC
11g.2572878_2572883delCA916079942KCNQ1c.552_557del (p.Gly185_Leu186del)
c.478-10557_478-10552del (n.478-10557_478-10552del)
c.813_818del (p.Gly272_Leu273del)
c.432_437del (p.Gly145_Leu146del)
c.124-10557_124-10552del (n.124-10557_124-10552del)
ClinVar dbSNP
11g.2572876C>ACA379131360KCNQ1c.550C>A (p.Leu184Met)
c.478-10559C>A (n.478-10559C>A)
c.811C>A (p.Leu271Met)
c.430C>A (p.Leu144Met)
c.124-10559C>A (n.124-10559C>A)
11g.2572876C=CA1948243185KCNQ1c.550C= (p.Leu184=)
c.478-10559C= (n.478-10559C=)
c.811C= (p.Leu271=)
c.430C= (p.Leu144=)
c.124-10559C= (n.124-10559C=)
11g.2572876C>GCA379131362KCNQ1c.550C>G (p.Leu184Val)
c.478-10559C>G (n.478-10559C>G)
c.811C>G (p.Leu271Val)
c.430C>G (p.Leu144Val)
c.124-10559C>G (n.124-10559C>G)
11g.2572876C>TCA008310KCNQ1c.550C>T (p.Leu184=)
c.478-10559C>T (n.478-10559C>T)
c.811C>T (p.Leu271=)
c.430C>T (p.Leu144=)
c.124-10559C>T (n.124-10559C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.2572877T>ACA379131370KCNQ1c.551T>A (p.Leu184Gln)
c.478-10558T>A (n.478-10558T>A)
c.812T>A (p.Leu271Gln)
c.431T>A (p.Leu144Gln)
c.124-10558T>A (n.124-10558T>A)
11g.2572877T>CCA379131368KCNQ1c.551T>C (p.Leu184Pro)
c.478-10558T>C (n.478-10558T>C)
c.812T>C (p.Leu271Pro)
c.431T>C (p.Leu144Pro)
c.124-10558T>C (n.124-10558T>C)
11g.2572877T>GCA379131366KCNQ1c.551T>G (p.Leu184Arg)
c.478-10558T>G (n.478-10558T>G)
c.812T>G (p.Leu271Arg)
c.431T>G (p.Leu144Arg)
c.124-10558T>G (n.124-10558T>G)
11g.2572878G>ACA472038144KCNQ1c.552G>A (p.Leu184=)
c.478-10557G>A (n.478-10557G>A)
c.813G>A (p.Leu271=)
c.432G>A (p.Leu144=)
c.124-10557G>A (n.124-10557G>A)
gnomAD v4
11g.2572878G>CCA472038145KCNQ1c.552G>C (p.Leu184=)
c.478-10557G>C (n.478-10557G>C)
c.813G>C (p.Leu271=)
c.432G>C (p.Leu144=)
c.124-10557G>C (n.124-10557G>C)
11g.2572878G>TCA472038146KCNQ1c.552G>T (p.Leu184=)
c.478-10557G>T (n.478-10557G>T)
c.813G>T (p.Leu271=)
c.432G>T (p.Leu144=)
c.124-10557G>T (n.124-10557G>T)
11g.2572879G>ACA040822KCNQ1c.553G>A (p.Gly185Ser)
c.478-10556G>A (n.478-10556G>A)
c.814G>A (p.Gly272Ser)
c.433G>A (p.Gly145Ser)
c.124-10556G>A (n.124-10556G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2572879G>CCA379131373KCNQ1c.553G>C (p.Gly185Arg)
c.478-10556G>C (n.478-10556G>C)
c.814G>C (p.Gly272Arg)
c.433G>C (p.Gly145Arg)
c.124-10556G>C (n.124-10556G>C)
11g.2572879G=CA1948243186KCNQ1c.553G= (p.Gly185=)
c.478-10556G= (n.478-10556G=)
c.814G= (p.Gly272=)
c.433G= (p.Gly145=)
c.124-10556G= (n.124-10556G=)
11g.2572879G>TCA379131374KCNQ1c.553G>T (p.Gly185Cys)
c.478-10556G>T (n.478-10556G>T)
c.814G>T (p.Gly272Cys)
c.433G>T (p.Gly145Cys)
c.124-10556G>T (n.124-10556G>T)
11g.2572880G>ACA008316KCNQ1c.554G>A (p.Gly185Asp)
c.478-10555G>A (n.478-10555G>A)
c.815G>A (p.Gly272Asp)
c.434G>A (p.Gly145Asp)
c.124-10555G>A (n.124-10555G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2572880G>CCA379131377KCNQ1c.554G>C (p.Gly185Ala)
c.478-10555G>C (n.478-10555G>C)
c.815G>C (p.Gly272Ala)
c.434G>C (p.Gly145Ala)
c.124-10555G>C (n.124-10555G>C)
11g.2572880G=CA1948243187KCNQ1c.554G= (p.Gly185=)
c.478-10555G= (n.478-10555G=)
c.815G= (p.Gly272=)
c.434G= (p.Gly145=)
c.124-10555G= (n.124-10555G=)
11g.2572880G>TCA008323KCNQ1c.554G>T (p.Gly185Val)
c.478-10555G>T (n.478-10555G>T)
c.815G>T (p.Gly272Val)
c.434G>T (p.Gly145Val)
c.124-10555G>T (n.124-10555G>T)
ClinVar dbSNP gnomAD v4
11g.2572881C>ACA472038147KCNQ1c.555C>A (p.Gly185=)
c.478-10554C>A (n.478-10554C>A)
c.816C>A (p.Gly272=)
c.435C>A (p.Gly145=)
c.124-10554C>A (n.124-10554C>A)
11g.2572881C>GCA472038148KCNQ1c.555C>G (p.Gly185=)
c.478-10554C>G (n.478-10554C>G)
c.816C>G (p.Gly272=)
c.435C>G (p.Gly145=)
c.124-10554C>G (n.124-10554C>G)
11g.2572881C>TCA472038149KCNQ1c.555C>T (p.Gly185=)
c.478-10554C>T (n.478-10554C>T)
c.816C>T (p.Gly272=)
c.435C>T (p.Gly145=)
c.124-10554C>T (n.124-10554C>T)
11g.2572885_2572895delCA2695213157KCNQ1c.559_569del (p.Ile187ValfsTer7)
c.478-10550_478-10540del (n.478-10550_478-10540del)
c.820_830del (p.Ile274ValfsTer7)
c.439_449del (p.Ile147ValfsTer7)
c.124-10550_124-10540del (n.124-10550_124-10540del)
c.559_569del (p.Ile187ValfsTer?)
11g.2572882C>ACA379131383KCNQ1c.556C>A (p.Leu186Ile)
c.478-10553C>A (n.478-10553C>A)
c.817C>A (p.Leu273Ile)
c.436C>A (p.Leu146Ile)
c.124-10553C>A (n.124-10553C>A)
11g.2572882C=CA1948243188KCNQ1c.556C= (p.Leu186=)
c.478-10553C= (n.478-10553C=)
c.817C= (p.Leu273=)
c.436C= (p.Leu146=)
c.124-10553C= (n.124-10553C=)
11g.2572882C>GCA379131380KCNQ1c.556C>G (p.Leu186Val)
c.478-10553C>G (n.478-10553C>G)
c.817C>G (p.Leu273Val)
c.436C>G (p.Leu146Val)
c.124-10553C>G (n.124-10553C>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.2572882C>TCA008331KCNQ1c.556C>T (p.Leu186Phe)
c.478-10553C>T (n.478-10553C>T)
c.817C>T (p.Leu273Phe)
c.436C>T (p.Leu146Phe)
c.124-10553C>T (n.124-10553C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2572883T>ACA379131385KCNQ1c.557T>A (p.Leu186His)
c.478-10552T>A (n.478-10552T>A)
c.818T>A (p.Leu273His)
c.437T>A (p.Leu146His)
c.124-10552T>A (n.124-10552T>A)
11g.2572883T>CCA16613286KCNQ1c.557T>C (p.Leu186Pro)
c.478-10552T>C (n.478-10552T>C)
c.818T>C (p.Leu273Pro)
c.437T>C (p.Leu146Pro)
c.124-10552T>C (n.124-10552T>C)
ClinVar dbSNP

Number of alleles fetched