Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.47449338T>ACA516373002ZNF41c.432A>T (p.Leu144=)
c.462A>T (p.Leu154=)
n.585A>T
c.174A>T (p.Leu58=)
c.534A>T (p.Leu178=)
c.438A>T (p.Leu146=)
c.558A>T (p.Leu186=)
c.330A>T (p.Leu110=)
c.324A>T (p.Leu108=)
Xg.47449338T>CCA516373003ZNF41c.432A>G (p.Leu144=)
c.462A>G (p.Leu154=)
n.585A>G
c.174A>G (p.Leu58=)
c.534A>G (p.Leu178=)
c.438A>G (p.Leu146=)
c.558A>G (p.Leu186=)
c.330A>G (p.Leu110=)
c.324A>G (p.Leu108=)
gnomAD v4
Xg.47449338T>GCA516373004ZNF41c.432A>C (p.Leu144=)
c.462A>C (p.Leu154=)
n.585A>C
c.174A>C (p.Leu58=)
c.534A>C (p.Leu178=)
c.438A>C (p.Leu146=)
c.558A>C (p.Leu186=)
c.330A>C (p.Leu110=)
c.324A>C (p.Leu108=)
Xg.47449339A>CCA413058129ZNF41c.431T>G (p.Leu144Arg)
c.461T>G (p.Leu154Arg)
n.584T>G
c.173T>G (p.Leu58Arg)
c.533T>G (p.Leu178Arg)
c.437T>G (p.Leu146Arg)
c.557T>G (p.Leu186Arg)
c.329T>G (p.Leu110Arg)
c.323T>G (p.Leu108Arg)
Xg.47449339A>GCA413058132ZNF41c.431T>C (p.Leu144Pro)
c.461T>C (p.Leu154Pro)
n.584T>C
c.173T>C (p.Leu58Pro)
c.533T>C (p.Leu178Pro)
c.437T>C (p.Leu146Pro)
c.557T>C (p.Leu186Pro)
c.329T>C (p.Leu110Pro)
c.323T>C (p.Leu108Pro)
Xg.47449339A>TCA413058130ZNF41c.431T>A (p.Leu144Gln)
c.461T>A (p.Leu154Gln)
n.584T>A
c.173T>A (p.Leu58Gln)
c.533T>A (p.Leu178Gln)
c.437T>A (p.Leu146Gln)
c.557T>A (p.Leu186Gln)
c.329T>A (p.Leu110Gln)
c.323T>A (p.Leu108Gln)
Xg.47449340G>ACA516373006ZNF41c.430C>T (p.Leu144=)
c.460C>T (p.Leu154=)
n.583C>T
c.172C>T (p.Leu58=)
c.532C>T (p.Leu178=)
c.436C>T (p.Leu146=)
c.556C>T (p.Leu186=)
c.328C>T (p.Leu110=)
c.322C>T (p.Leu108=)
Xg.47449340G>CCA413058134ZNF41c.430C>G (p.Leu144Val)
c.460C>G (p.Leu154Val)
n.583C>G
c.172C>G (p.Leu58Val)
c.532C>G (p.Leu178Val)
c.436C>G (p.Leu146Val)
c.556C>G (p.Leu186Val)
c.328C>G (p.Leu110Val)
c.322C>G (p.Leu108Val)
dbSNP
Xg.47449340G=CA2427930877ZNF41c.430C= (p.Leu144=)
c.460C= (p.Leu154=)
n.583C=
c.172C= (p.Leu58=)
c.532C= (p.Leu178=)
c.436C= (p.Leu146=)
c.556C= (p.Leu186=)
c.328C= (p.Leu110=)
c.322C= (p.Leu108=)
Xg.47449340G>TCA413058136ZNF41c.430C>A (p.Leu144Ile)
c.460C>A (p.Leu154Ile)
n.583C>A
c.172C>A (p.Leu58Ile)
c.532C>A (p.Leu178Ile)
c.436C>A (p.Leu146Ile)
c.556C>A (p.Leu186Ile)
c.328C>A (p.Leu110Ile)
c.322C>A (p.Leu108Ile)
Xg.47449341C>ACA413058137ZNF41c.429G>T (p.Gln143His)
c.459G>T (p.Gln153His)
n.582G>T
c.171G>T (p.Gln57His)
c.531G>T (p.Gln177His)
c.435G>T (p.Gln145His)
c.555G>T (p.Gln185His)
c.327G>T (p.Gln109His)
c.321G>T (p.Gln107His)
Xg.47449341C>GCA413058139ZNF41c.429G>C (p.Gln143His)
c.459G>C (p.Gln153His)
n.582G>C
c.171G>C (p.Gln57His)
c.531G>C (p.Gln177His)
c.435G>C (p.Gln145His)
c.555G>C (p.Gln185His)
c.327G>C (p.Gln109His)
c.321G>C (p.Gln107His)
Xg.47449341C>TCA516373007ZNF41c.429G>A (p.Gln143=)
c.459G>A (p.Gln153=)
n.582G>A
c.171G>A (p.Gln57=)
c.531G>A (p.Gln177=)
c.435G>A (p.Gln145=)
c.555G>A (p.Gln185=)
c.327G>A (p.Gln109=)
c.321G>A (p.Gln107=)
gnomAD v4
Xg.47449342T>ACA413058141ZNF41c.428A>T (p.Gln143Leu)
c.458A>T (p.Gln153Leu)
n.581A>T
c.170A>T (p.Gln57Leu)
c.530A>T (p.Gln177Leu)
c.434A>T (p.Gln145Leu)
c.554A>T (p.Gln185Leu)
c.326A>T (p.Gln109Leu)
c.320A>T (p.Gln107Leu)
Xg.47449342T>CCA413058143ZNF41c.428A>G (p.Gln143Arg)
c.458A>G (p.Gln153Arg)
n.581A>G
c.170A>G (p.Gln57Arg)
c.530A>G (p.Gln177Arg)
c.434A>G (p.Gln145Arg)
c.554A>G (p.Gln185Arg)
c.326A>G (p.Gln109Arg)
c.320A>G (p.Gln107Arg)
Xg.47449342T>GCA413058144ZNF41c.428A>C (p.Gln143Pro)
c.458A>C (p.Gln153Pro)
n.581A>C
c.170A>C (p.Gln57Pro)
c.530A>C (p.Gln177Pro)
c.434A>C (p.Gln145Pro)
c.554A>C (p.Gln185Pro)
c.326A>C (p.Gln109Pro)
c.320A>C (p.Gln107Pro)
Xg.47449343G>ACA413058147ZNF41c.427C>T (p.Gln143Ter)
c.457C>T (p.Gln153Ter)
n.580C>T
c.169C>T (p.Gln57Ter)
c.529C>T (p.Gln177Ter)
c.433C>T (p.Gln145Ter)
c.553C>T (p.Gln185Ter)
c.325C>T (p.Gln109Ter)
c.319C>T (p.Gln107Ter)
dbSNP gnomAD v4
Xg.47449343G>CCA413058149ZNF41c.427C>G (p.Gln143Glu)
c.457C>G (p.Gln153Glu)
n.580C>G
c.169C>G (p.Gln57Glu)
c.529C>G (p.Gln177Glu)
c.433C>G (p.Gln145Glu)
c.553C>G (p.Gln185Glu)
c.325C>G (p.Gln109Glu)
c.319C>G (p.Gln107Glu)
Xg.47449343G>TCA413058150ZNF41c.427C>A (p.Gln143Lys)
c.457C>A (p.Gln153Lys)
n.580C>A
c.169C>A (p.Gln57Lys)
c.529C>A (p.Gln177Lys)
c.433C>A (p.Gln145Lys)
c.553C>A (p.Gln185Lys)
c.325C>A (p.Gln109Lys)
c.319C>A (p.Gln107Lys)
Xg.47449344G>ACA516373009ZNF41c.426C>T (p.Asp142=)
c.456C>T (p.Asp152=)
n.579C>T
c.168C>T (p.Asp56=)
c.528C>T (p.Asp176=)
c.432C>T (p.Asp144=)
c.552C>T (p.Asp184=)
c.324C>T (p.Asp108=)
c.318C>T (p.Asp106=)
ClinVar
Xg.47449344G>CCA413058151ZNF41c.426C>G (p.Asp142Glu)
c.456C>G (p.Asp152Glu)
n.579C>G
c.168C>G (p.Asp56Glu)
c.528C>G (p.Asp176Glu)
c.432C>G (p.Asp144Glu)
c.552C>G (p.Asp184Glu)
c.324C>G (p.Asp108Glu)
c.318C>G (p.Asp106Glu)
Xg.47449344G>TCA413058153ZNF41c.426C>A (p.Asp142Glu)
c.456C>A (p.Asp152Glu)
n.579C>A
c.168C>A (p.Asp56Glu)
c.528C>A (p.Asp176Glu)
c.432C>A (p.Asp144Glu)
c.552C>A (p.Asp184Glu)
c.324C>A (p.Asp108Glu)
c.318C>A (p.Asp106Glu)
Xg.47449345T>ACA413058158ZNF41c.425A>T (p.Asp142Val)
c.455A>T (p.Asp152Val)
n.578A>T
c.167A>T (p.Asp56Val)
c.527A>T (p.Asp176Val)
c.431A>T (p.Asp144Val)
c.551A>T (p.Asp184Val)
c.323A>T (p.Asp108Val)
c.317A>T (p.Asp106Val)
Xg.47449345T>CCA413058155ZNF41c.425A>G (p.Asp142Gly)
c.455A>G (p.Asp152Gly)
n.578A>G
c.167A>G (p.Asp56Gly)
c.527A>G (p.Asp176Gly)
c.431A>G (p.Asp144Gly)
c.551A>G (p.Asp184Gly)
c.323A>G (p.Asp108Gly)
c.317A>G (p.Asp106Gly)
Xg.47449345T>GCA413058156ZNF41c.425A>C (p.Asp142Ala)
c.455A>C (p.Asp152Ala)
n.578A>C
c.167A>C (p.Asp56Ala)
c.527A>C (p.Asp176Ala)
c.431A>C (p.Asp144Ala)
c.551A>C (p.Asp184Ala)
c.323A>C (p.Asp108Ala)
c.317A>C (p.Asp106Ala)
Xg.47449346C>ACA413058160ZNF41c.424G>T (p.Asp142Tyr)
c.454G>T (p.Asp152Tyr)
n.577G>T
c.166G>T (p.Asp56Tyr)
c.526G>T (p.Asp176Tyr)
c.430G>T (p.Asp144Tyr)
c.550G>T (p.Asp184Tyr)
c.322G>T (p.Asp108Tyr)
c.316G>T (p.Asp106Tyr)
dbSNP
Xg.47449346C=CA2427930878ZNF41c.424G= (p.Asp142=)
c.454G= (p.Asp152=)
n.577G=
c.166G= (p.Asp56=)
c.526G= (p.Asp176=)
c.430G= (p.Asp144=)
c.550G= (p.Asp184=)
c.322G= (p.Asp108=)
c.316G= (p.Asp106=)
Xg.47449346C>GCA413058161ZNF41c.424G>C (p.Asp142His)
c.454G>C (p.Asp152His)
n.577G>C
c.166G>C (p.Asp56His)
c.526G>C (p.Asp176His)
c.430G>C (p.Asp144His)
c.550G>C (p.Asp184His)
c.322G>C (p.Asp108His)
c.316G>C (p.Asp106His)
Xg.47449346C>TCA10397796ZNF41c.424G>A (p.Asp142Asn)
c.454G>A (p.Asp152Asn)
n.577G>A
c.166G>A (p.Asp56Asn)
c.526G>A (p.Asp176Asn)
c.430G>A (p.Asp144Asn)
c.550G>A (p.Asp184Asn)
c.322G>A (p.Asp108Asn)
c.316G>A (p.Asp106Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47449347A>CCA413058164ZNF41c.423T>G (p.Asn141Lys)
c.453T>G (p.Asn151Lys)
n.576T>G
c.165T>G (p.Asn55Lys)
c.525T>G (p.Asn175Lys)
c.429T>G (p.Asn143Lys)
c.549T>G (p.Asn183Lys)
c.321T>G (p.Asn107Lys)
c.315T>G (p.Asn105Lys)
Xg.47449347A>GCA516373011ZNF41c.423T>C (p.Asn141=)
c.453T>C (p.Asn151=)
n.576T>C
c.165T>C (p.Asn55=)
c.525T>C (p.Asn175=)
c.429T>C (p.Asn143=)
c.549T>C (p.Asn183=)
c.321T>C (p.Asn107=)
c.315T>C (p.Asn105=)
Xg.47449347A>TCA413058166ZNF41c.423T>A (p.Asn141Lys)
c.453T>A (p.Asn151Lys)
n.576T>A
c.165T>A (p.Asn55Lys)
c.525T>A (p.Asn175Lys)
c.429T>A (p.Asn143Lys)
c.549T>A (p.Asn183Lys)
c.321T>A (p.Asn107Lys)
c.315T>A (p.Asn105Lys)
Xg.47449348T>ACA413058168ZNF41c.422A>T (p.Asn141Ile)
c.452A>T (p.Asn151Ile)
n.575A>T
c.164A>T (p.Asn55Ile)
c.524A>T (p.Asn175Ile)
c.428A>T (p.Asn143Ile)
c.548A>T (p.Asn183Ile)
c.320A>T (p.Asn107Ile)
c.314A>T (p.Asn105Ile)
Xg.47449348T>CCA413058169ZNF41c.422A>G (p.Asn141Ser)
c.452A>G (p.Asn151Ser)
n.575A>G
c.164A>G (p.Asn55Ser)
c.524A>G (p.Asn175Ser)
c.428A>G (p.Asn143Ser)
c.548A>G (p.Asn183Ser)
c.320A>G (p.Asn107Ser)
c.314A>G (p.Asn105Ser)
Xg.47449348T>GCA413058171ZNF41c.422A>C (p.Asn141Thr)
c.452A>C (p.Asn151Thr)
n.575A>C
c.164A>C (p.Asn55Thr)
c.524A>C (p.Asn175Thr)
c.428A>C (p.Asn143Thr)
c.548A>C (p.Asn183Thr)
c.320A>C (p.Asn107Thr)
c.314A>C (p.Asn105Thr)
Xg.47449349T>ACA413058173ZNF41c.421A>T (p.Asn141Tyr)
c.451A>T (p.Asn151Tyr)
n.574A>T
c.163A>T (p.Asn55Tyr)
c.523A>T (p.Asn175Tyr)
c.427A>T (p.Asn143Tyr)
c.547A>T (p.Asn183Tyr)
c.319A>T (p.Asn107Tyr)
c.313A>T (p.Asn105Tyr)
Xg.47449349T>CCA413058174ZNF41c.421A>G (p.Asn141Asp)
c.451A>G (p.Asn151Asp)
n.574A>G
c.163A>G (p.Asn55Asp)
c.523A>G (p.Asn175Asp)
c.427A>G (p.Asn143Asp)
c.547A>G (p.Asn183Asp)
c.319A>G (p.Asn107Asp)
c.313A>G (p.Asn105Asp)
Xg.47449349T>GCA413058175ZNF41c.421A>C (p.Asn141His)
c.451A>C (p.Asn151His)
n.574A>C
c.163A>C (p.Asn55His)
c.523A>C (p.Asn175His)
c.427A>C (p.Asn143His)
c.547A>C (p.Asn183His)
c.319A>C (p.Asn107His)
c.313A>C (p.Asn105His)
Xg.47449350A>CCA413058177ZNF41c.420T>G (p.Asp140Glu)
c.450T>G (p.Asp150Glu)
n.573T>G
c.162T>G (p.Asp54Glu)
c.522T>G (p.Asp174Glu)
c.426T>G (p.Asp142Glu)
c.546T>G (p.Asp182Glu)
c.318T>G (p.Asp106Glu)
c.312T>G (p.Asp104Glu)
Xg.47449350A>GCA516373013ZNF41c.420T>C (p.Asp140=)
c.450T>C (p.Asp150=)
n.573T>C
c.162T>C (p.Asp54=)
c.522T>C (p.Asp174=)
c.426T>C (p.Asp142=)
c.546T>C (p.Asp182=)
c.318T>C (p.Asp106=)
c.312T>C (p.Asp104=)
Xg.47449350A>TCA413058179ZNF41c.420T>A (p.Asp140Glu)
c.450T>A (p.Asp150Glu)
n.573T>A
c.162T>A (p.Asp54Glu)
c.522T>A (p.Asp174Glu)
c.426T>A (p.Asp142Glu)
c.546T>A (p.Asp182Glu)
c.318T>A (p.Asp106Glu)
c.312T>A (p.Asp104Glu)
Xg.47449351T>ACA413058181ZNF41c.419A>T (p.Asp140Val)
c.449A>T (p.Asp150Val)
n.572A>T
c.161A>T (p.Asp54Val)
c.521A>T (p.Asp174Val)
c.425A>T (p.Asp142Val)
c.545A>T (p.Asp182Val)
c.317A>T (p.Asp106Val)
c.311A>T (p.Asp104Val)
Xg.47449351T>CCA413058182ZNF41c.419A>G (p.Asp140Gly)
c.449A>G (p.Asp150Gly)
n.572A>G
c.161A>G (p.Asp54Gly)
c.521A>G (p.Asp174Gly)
c.425A>G (p.Asp142Gly)
c.545A>G (p.Asp182Gly)
c.317A>G (p.Asp106Gly)
c.311A>G (p.Asp104Gly)
Xg.47449351T>GCA413058184ZNF41c.419A>C (p.Asp140Ala)
c.449A>C (p.Asp150Ala)
n.572A>C
c.161A>C (p.Asp54Ala)
c.521A>C (p.Asp174Ala)
c.425A>C (p.Asp142Ala)
c.545A>C (p.Asp182Ala)
c.317A>C (p.Asp106Ala)
c.311A>C (p.Asp104Ala)
Xg.47449352C>ACA413058186ZNF41c.418G>T (p.Asp140Tyr)
c.448G>T (p.Asp150Tyr)
n.571G>T
c.160G>T (p.Asp54Tyr)
c.520G>T (p.Asp174Tyr)
c.424G>T (p.Asp142Tyr)
c.544G>T (p.Asp182Tyr)
c.316G>T (p.Asp106Tyr)
c.310G>T (p.Asp104Tyr)
Xg.47449352C=CA2427930879ZNF41c.418G= (p.Asp140=)
c.448G= (p.Asp150=)
n.571G=
c.160G= (p.Asp54=)
c.520G= (p.Asp174=)
c.424G= (p.Asp142=)
c.544G= (p.Asp182=)
c.316G= (p.Asp106=)
c.310G= (p.Asp104=)
Xg.47449352C>GCA413058188ZNF41c.418G>C (p.Asp140His)
c.448G>C (p.Asp150His)
n.571G>C
c.160G>C (p.Asp54His)
c.520G>C (p.Asp174His)
c.424G>C (p.Asp142His)
c.544G>C (p.Asp182His)
c.316G>C (p.Asp106His)
c.310G>C (p.Asp104His)
dbSNP gnomAD v2 gnomAD v4
Xg.47449352C>TCA413058190ZNF41c.418G>A (p.Asp140Asn)
c.448G>A (p.Asp150Asn)
n.571G>A
c.160G>A (p.Asp54Asn)
c.520G>A (p.Asp174Asn)
c.424G>A (p.Asp142Asn)
c.544G>A (p.Asp182Asn)
c.316G>A (p.Asp106Asn)
c.310G>A (p.Asp104Asn)
Xg.47449353T>ACA413058194ZNF41c.417A>T (p.Gln139His)
c.447A>T (p.Gln149His)
n.570A>T
c.159A>T (p.Gln53His)
c.519A>T (p.Gln173His)
c.423A>T (p.Gln141His)
c.543A>T (p.Gln181His)
c.315A>T (p.Gln105His)
c.309A>T (p.Gln103His)
Xg.47449353T>CCA516373015ZNF41c.417A>G (p.Gln139=)
c.447A>G (p.Gln149=)
n.570A>G
c.159A>G (p.Gln53=)
c.519A>G (p.Gln173=)
c.423A>G (p.Gln141=)
c.543A>G (p.Gln181=)
c.315A>G (p.Gln105=)
c.309A>G (p.Gln103=)

Number of alleles fetched