Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.88439171dupCA2634824424ZNF469c.11701dup (p.Leu3901ProfsTer15)
c.11617dup (p.Leu3873ProfsTer15)
gnomAD v4
16g.88439169C>ACA397131015ZNF469c.11699C>A (p.Pro3900His)
c.11615C>A (p.Pro3872His)
16g.88439169C=CA2241074382ZNF469c.11699C= (p.Pro3900=)
c.11615C= (p.Pro3872=)
16g.88439169C>GCA286388410ZNF469c.11699C>G (p.Pro3900Arg)
c.11615C>G (p.Pro3872Arg)
dbSNP
16g.88439169C>TCA151277ZNF469c.11699C>T (p.Pro3900Leu)
c.11615C>T (p.Pro3872Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439170C>ACA497359604ZNF469c.11700C>A (p.Pro3900=)
c.11616C>A (p.Pro3872=)
ClinVar
16g.88439170C=CA2241074385ZNF469c.11700C= (p.Pro3900=)
c.11616C= (p.Pro3872=)
16g.88439170C>GCA497359605ZNF469c.11700C>G (p.Pro3900=)
c.11616C>G (p.Pro3872=)
16g.88439170C>TCA497359606ZNF469c.11700C>T (p.Pro3900=)
c.11616C>T (p.Pro3872=)
dbSNP gnomAD v4
16g.88439171C>ACA397131017ZNF469c.11701C>A (p.Leu3901Met)
c.11617C>A (p.Leu3873Met)
16g.88439171C=CA2241074387ZNF469c.11701C= (p.Leu3901=)
c.11617C= (p.Leu3873=)
16g.88439171C>GCA397131018ZNF469c.11701C>G (p.Leu3901Val)
c.11617C>G (p.Leu3873Val)
16g.88439171C>TCA497359607ZNF469c.11701C>T (p.Leu3901=)
c.11617C>T (p.Leu3873=)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88439172T>ACA397131020ZNF469c.11702T>A (p.Leu3901Gln)
c.11618T>A (p.Leu3873Gln)
16g.88439172T>CCA397131021ZNF469c.11702T>C (p.Leu3901Pro)
c.11618T>C (p.Leu3873Pro)
16g.88439172T>GCA397131023ZNF469c.11702T>G (p.Leu3901Arg)
c.11618T>G (p.Leu3873Arg)
16g.88439173G>ACA497359613ZNF469c.11703G>A (p.Leu3901=)
c.11619G>A (p.Leu3873=)
gnomAD v4
16g.88439173G>CCA497359614ZNF469c.11703G>C (p.Leu3901=)
c.11619G>C (p.Leu3873=)
gnomAD v4
16g.88439173G>TCA497359615ZNF469c.11703G>T (p.Leu3901=)
c.11619G>T (p.Leu3873=)
gnomAD v4
16g.88439174C>ACA397131026ZNF469c.11704C>A (p.Leu3902Ile)
c.11620C>A (p.Leu3874Ile)
16g.88439174C=CA2241074390ZNF469c.11704C= (p.Leu3902=)
c.11620C= (p.Leu3874=)
16g.88439174C>GCA397131024ZNF469c.11704C>G (p.Leu3902Val)
c.11620C>G (p.Leu3874Val)
16g.88439174C>TCA397131025ZNF469c.11704C>T (p.Leu3902Phe)
c.11620C>T (p.Leu3874Phe)
dbSNP gnomAD v2
16g.88439175T>ACA397131027ZNF469c.11705T>A (p.Leu3902His)
c.11621T>A (p.Leu3874His)
16g.88439175T>CCA397131028ZNF469c.11705T>C (p.Leu3902Pro)
c.11621T>C (p.Leu3874Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439175T>GCA397131030ZNF469c.11705T>G (p.Leu3902Arg)
c.11621T>G (p.Leu3874Arg)
16g.88439175T=CA2241074393ZNF469c.11705T= (p.Leu3902=)
c.11621T= (p.Leu3874=)
16g.88439176C>ACA497359616ZNF469c.11706C>A (p.Leu3902=)
c.11622C>A (p.Leu3874=)
16g.88439176C=CA2241074394ZNF469c.11706C= (p.Leu3902=)
c.11622C= (p.Leu3874=)
16g.88439176C>GCA497359617ZNF469c.11706C>G (p.Leu3902=)
c.11622C>G (p.Leu3874=)
gnomAD v4
16g.88439176C>TCA497359618ZNF469c.11706C>T (p.Leu3902=)
c.11622C>T (p.Leu3874=)
dbSNP gnomAD v2 gnomAD v4
16g.88439177A>CCA497359619ZNF469c.11707A>C (p.Arg3903=)
c.11623A>C (p.Arg3875=)
gnomAD v4
16g.88439177A>GCA397131032ZNF469c.11707A>G (p.Arg3903Gly)
c.11623A>G (p.Arg3875Gly)
16g.88439177A>TCA397131034ZNF469c.11707A>T (p.Arg3903Trp)
c.11623A>T (p.Arg3875Trp)
16g.88439178G>ACA397131038ZNF469c.11708G>A (p.Arg3903Lys)
c.11624G>A (p.Arg3875Lys)
dbSNP gnomAD v2 gnomAD v4
16g.88439178G>CCA397131037ZNF469c.11708G>C (p.Arg3903Thr)
c.11624G>C (p.Arg3875Thr)
16g.88439178G=CA2241074396ZNF469c.11708G= (p.Arg3903=)
c.11624G= (p.Arg3875=)
16g.88439178G>TCA397131035ZNF469c.11708G>T (p.Arg3903Met)
c.11624G>T (p.Arg3875Met)
dbSNP gnomAD v3 gnomAD v4
16g.88439179G>ACA497359621ZNF469c.11709G>A (p.Arg3903=)
c.11625G>A (p.Arg3875=)
ClinVar dbSNP
16g.88439179G>CCA397131040ZNF469c.11709G>C (p.Arg3903Ser)
c.11625G>C (p.Arg3875Ser)
16g.88439179G=CA2241074399ZNF469c.11709G= (p.Arg3903=)
c.11625G= (p.Arg3875=)
16g.88439179G>TCA397131041ZNF469c.11709G>T (p.Arg3903Ser)
c.11625G>T (p.Arg3875Ser)
dbSNP gnomAD v2 gnomAD v4
16g.88439179_88439180delinsGCCA2241074398ZNF469c.11709_11710delinsGC (p.Arg3903=)
c.11625_11626delinsGC (p.Arg3875=)
16g.88439180C>ACA397131042ZNF469c.11710C>A (p.Pro3904Thr)
c.11626C>A (p.Pro3876Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439180C=CA2241074405ZNF469c.11710C= (p.Pro3904=)
c.11626C= (p.Pro3876=)
16g.88439180C>GCA397131043ZNF469c.11710C>G (p.Pro3904Ala)
c.11626C>G (p.Pro3876Ala)
ClinVar gnomAD v4
16g.88439180C>TCA397131045ZNF469c.11710C>T (p.Pro3904Ser)
c.11626C>T (p.Pro3876Ser)
gnomAD v4
16g.88439180_88439181delinsTTCA645580423ZNF469c.11710_11711delinsTT (p.Pro3904Phe)
c.11626_11627delinsTT (p.Pro3876Phe)
COSMIC
16g.88439185dupCA2808056659ZNF469c.11715dup (p.Lys3906GlnfsTer10)
c.11631dup (p.Lys3878GlnfsTer10)
16g.88439185delCA624447664ZNF469c.11715del (p.Lys3906ArgfsTer?)
c.11631del (p.Lys3878ArgfsTer?)
dbSNP gnomAD v2 gnomAD v4
16g.88439183_88439185delCA2634824427ZNF469c.11713_11715del (p.Pro3905del)
c.11629_11631del (p.Pro3877del)
gnomAD v4
16g.88439181C>ACA397131046ZNF469c.11711C>A (p.Pro3904His)
c.11627C>A (p.Pro3876His)
dbSNP gnomAD v2 gnomAD v4
16g.88439181C=CA2241074409ZNF469c.11711C= (p.Pro3904=)
c.11627C= (p.Pro3876=)
16g.88439181C>GCA397131048ZNF469c.11711C>G (p.Pro3904Arg)
c.11627C>G (p.Pro3876Arg)
16g.88439181C>TCA397131049ZNF469c.11711C>T (p.Pro3904Leu)
c.11627C>T (p.Pro3876Leu)
dbSNP gnomAD v3 gnomAD v4
16g.88439182C>ACA497359627ZNF469c.11712C>A (p.Pro3904=)
c.11628C>A (p.Pro3876=)
16g.88439182C=CA2241074411ZNF469c.11712C= (p.Pro3904=)
c.11628C= (p.Pro3876=)
16g.88439182C>GCA497359630ZNF469c.11712C>G (p.Pro3904=)
c.11628C>G (p.Pro3876=)
16g.88439182C>TCA497359631ZNF469c.11712C>T (p.Pro3904=)
c.11628C>T (p.Pro3876=)
dbSNP gnomAD v2 gnomAD v4
16g.88439183C>ACA397131050ZNF469c.11713C>A (p.Pro3905Thr)
c.11629C>A (p.Pro3877Thr)
16g.88439183C=CA2241074414ZNF469c.11713C= (p.Pro3905=)
c.11629C= (p.Pro3877=)
16g.88439183C>GCA397131051ZNF469c.11713C>G (p.Pro3905Ala)
c.11629C>G (p.Pro3877Ala)
16g.88439183C>TCA397131053ZNF469c.11713C>T (p.Pro3905Ser)
c.11629C>T (p.Pro3877Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439184C>ACA397131055ZNF469c.11714C>A (p.Pro3905His)
c.11630C>A (p.Pro3877His)
ClinVar gnomAD v4
16g.88439184C=CA2241074418ZNF469c.11714C= (p.Pro3905=)
c.11630C= (p.Pro3877=)
16g.88439184C>GCA397131057ZNF469c.11714C>G (p.Pro3905Arg)
c.11630C>G (p.Pro3877Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439184C>TCA286388422ZNF469c.11714C>T (p.Pro3905Leu)
c.11630C>T (p.Pro3877Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439184_88439185delinsATCA2580092242ZNF469c.11714_11715delinsAT (p.Pro3905His)
c.11630_11631delinsAT (p.Pro3877His)
ClinVar dbSNP
16g.88439185C>ACA286388425ZNF469c.11715C>A (p.Pro3905=)
c.11631C>A (p.Pro3877=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439185C=CA2241074423ZNF469c.11715C= (p.Pro3905=)
c.11631C= (p.Pro3877=)
16g.88439185C>GCA286388427ZNF469c.11715C>G (p.Pro3905=)
c.11631C>G (p.Pro3877=)
ClinVar dbSNP gnomAD v4
16g.88439185C>TCA497359632ZNF469c.11715C>T (p.Pro3905=)
c.11631C>T (p.Pro3877=)
ClinVar dbSNP
16g.88439186A>CCA397131063ZNF469c.11716A>C (p.Lys3906Gln)
c.11632A>C (p.Lys3878Gln)
16g.88439186A>GCA397131061ZNF469c.11716A>G (p.Lys3906Glu)
c.11632A>G (p.Lys3878Glu)
16g.88439186A>TCA397131060ZNF469c.11716A>T (p.Lys3906Ter)
c.11632A>T (p.Lys3878Ter)
16g.88439187A=CA2241074425ZNF469c.11717A= (p.Lys3906=)
c.11633A= (p.Lys3878=)
16g.88439187A>CCA397131064ZNF469c.11717A>C (p.Lys3906Thr)
c.11633A>C (p.Lys3878Thr)
dbSNP gnomAD v3 gnomAD v4
16g.88439187A>GCA397131065ZNF469c.11717A>G (p.Lys3906Arg)
c.11633A>G (p.Lys3878Arg)
ClinVar gnomAD v4
16g.88439187A>TCA397131067ZNF469c.11717A>T (p.Lys3906Met)
c.11633A>T (p.Lys3878Met)
gnomAD v4
16g.88439188G>ACA497359648ZNF469c.11718G>A (p.Lys3906=)
c.11634G>A (p.Lys3878=)
dbSNP
16g.88439188G>CCA397131068ZNF469c.11718G>C (p.Lys3906Asn)
c.11634G>C (p.Lys3878Asn)
16g.88439188G>TCA397131069ZNF469c.11718G>T (p.Lys3906Asn)
c.11634G>T (p.Lys3878Asn)
16g.88439189A>CCA497359651ZNF469c.11719A>C (p.Arg3907=)
c.11635A>C (p.Arg3879=)
16g.88439189A>GCA397131071ZNF469c.11719A>G (p.Arg3907Gly)
c.11635A>G (p.Arg3879Gly)
16g.88439189A>TCA397131072ZNF469c.11719A>T (p.Arg3907Trp)
c.11635A>T (p.Arg3879Trp)
16g.88439190G>ACA397131073ZNF469c.11720G>A (p.Arg3907Lys)
c.11636G>A (p.Arg3879Lys)
16g.88439190G>CCA397131075ZNF469c.11720G>C (p.Arg3907Thr)
c.11636G>C (p.Arg3879Thr)
16g.88439190G>TCA397131076ZNF469c.11720G>T (p.Arg3907Met)
c.11636G>T (p.Arg3879Met)
16g.88439193dupCA2634824430ZNF469c.11723dup (p.Thr3909HisfsTer7)
c.11639dup (p.Thr3881HisfsTer7)
gnomAD v4
16g.88439193delCA2634824431ZNF469c.11723del (p.Gly3908AlafsTer?)
c.11639del (p.Gly3880AlafsTer?)
gnomAD v4
16g.88439191G>ACA497359655ZNF469c.11721G>A (p.Arg3907=)
c.11637G>A (p.Arg3879=)
COSMIC
16g.88439191G>CCA397131078ZNF469c.11721G>C (p.Arg3907Ser)
c.11637G>C (p.Arg3879Ser)
16g.88439191G>TCA397131080ZNF469c.11721G>T (p.Arg3907Ser)
c.11637G>T (p.Arg3879Ser)
16g.88439192G>ACA397131084ZNF469c.11722G>A (p.Gly3908Ser)
c.11638G>A (p.Gly3880Ser)
ClinVar dbSNP
16g.88439192G>CCA397131083ZNF469c.11722G>C (p.Gly3908Arg)
c.11638G>C (p.Gly3880Arg)
16g.88439192G>TCA397131081ZNF469c.11722G>T (p.Gly3908Cys)
c.11638G>T (p.Gly3880Cys)
gnomAD v4
16g.88439193G>ACA286388433ZNF469c.11723G>A (p.Gly3908Asp)
c.11639G>A (p.Gly3880Asp)
dbSNP gnomAD v4
16g.88439193G>CCA397131087ZNF469c.11723G>C (p.Gly3908Ala)
c.11639G>C (p.Gly3880Ala)
gnomAD v4
16g.88439193G=CA2241074428ZNF469c.11723G= (p.Gly3908=)
c.11639G= (p.Gly3880=)
16g.88439193G>TCA397131086ZNF469c.11723G>T (p.Gly3908Val)
c.11639G>T (p.Gly3880Val)
16g.88439194C>ACA497359658ZNF469c.11724C>A (p.Gly3908=)
c.11640C>A (p.Gly3880=)
16g.88439194C>GCA497359660ZNF469c.11724C>G (p.Gly3908=)
c.11640C>G (p.Gly3880=)
16g.88439194C>TCA497359659ZNF469c.11724C>T (p.Gly3908=)
c.11640C>T (p.Gly3880=)
16g.88439195A>CCA397131089ZNF469c.11725A>C (p.Thr3909Pro)
c.11641A>C (p.Thr3881Pro)
16g.88439195A>GCA397131091ZNF469c.11725A>G (p.Thr3909Ala)
c.11641A>G (p.Thr3881Ala)
16g.88439195A>TCA397131092ZNF469c.11725A>T (p.Thr3909Ser)
c.11641A>T (p.Thr3881Ser)
16g.88439196C>ACA397131094ZNF469c.11726C>A (p.Thr3909Lys)
c.11642C>A (p.Thr3881Lys)
16g.88439196C>GCA397131095ZNF469c.11726C>G (p.Thr3909Arg)
c.11642C>G (p.Thr3881Arg)
dbSNP gnomAD v3 gnomAD v4
16g.88439196C>TCA397131097ZNF469c.11726C>T (p.Thr3909Ile)
c.11642C>T (p.Thr3881Ile)
16g.88439197A>CCA497359663ZNF469c.11727A>C (p.Thr3909=)
c.11643A>C (p.Thr3881=)
16g.88439197A>GCA497359664ZNF469c.11727A>G (p.Thr3909=)
c.11643A>G (p.Thr3881=)
gnomAD v4
16g.88439197A>TCA497359665ZNF469c.11727A>T (p.Thr3909=)
c.11643A>T (p.Thr3881=)
16g.88439198G>ACA397131101ZNF469c.11728G>A (p.Ala3910Thr)
c.11644G>A (p.Ala3882Thr)
16g.88439198G>CCA397131100ZNF469c.11728G>C (p.Ala3910Pro)
c.11644G>C (p.Ala3882Pro)
16g.88439198G>TCA397131099ZNF469c.11728G>T (p.Ala3910Ser)
c.11644G>T (p.Ala3882Ser)
16g.88439199C>ACA397131103ZNF469c.11729C>A (p.Ala3910Asp)
c.11645C>A (p.Ala3882Asp)
16g.88439199C>GCA397131105ZNF469c.11729C>G (p.Ala3910Gly)
c.11645C>G (p.Ala3882Gly)
16g.88439199C>TCA397131107ZNF469c.11729C>T (p.Ala3910Val)
c.11645C>T (p.Ala3882Val)
16g.88439200T>ACA497359667ZNF469c.11730T>A (p.Ala3910=)
c.11646T>A (p.Ala3882=)
16g.88439200T>CCA497359668ZNF469c.11730T>C (p.Ala3910=)
c.11646T>C (p.Ala3882=)
16g.88439200T>GCA497359670ZNF469c.11730T>G (p.Ala3910=)
c.11646T>G (p.Ala3882=)
16g.88439201G>ACA397131108ZNF469c.11731G>A (p.Val3911Ile)
c.11647G>A (p.Val3883Ile)
16g.88439201G>CCA397131110ZNF469c.11731G>C (p.Val3911Leu)
c.11647G>C (p.Val3883Leu)
16g.88439201G>TCA397131111ZNF469c.11731G>T (p.Val3911Phe)
c.11647G>T (p.Val3883Phe)
16g.88439202T>ACA397131112ZNF469c.11732T>A (p.Val3911Asp)
c.11648T>A (p.Val3883Asp)
16g.88439202T>CCA397131114ZNF469c.11732T>C (p.Val3911Ala)
c.11648T>C (p.Val3883Ala)
16g.88439202T>GCA397131113ZNF469c.11732T>G (p.Val3911Gly)
c.11648T>G (p.Val3883Gly)
16g.88439203C>ACA497359673ZNF469c.11733C>A (p.Val3911=)
c.11649C>A (p.Val3883=)
16g.88439203C=CA2241074429ZNF469c.11733C= (p.Val3911=)
c.11649C= (p.Val3883=)
16g.88439203C>GCA286388442ZNF469c.11733C>G (p.Val3911=)
c.11649C>G (p.Val3883=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439203C>TCA497359676ZNF469c.11733C>T (p.Val3911=)
c.11649C>T (p.Val3883=)
16g.88439204C>ACA397131115ZNF469c.11734C>A (p.His3912Asn)
c.11650C>A (p.His3884Asn)
16g.88439204C>GCA397131117ZNF469c.11734C>G (p.His3912Asp)
c.11650C>G (p.His3884Asp)
16g.88439204C>TCA397131118ZNF469c.11734C>T (p.His3912Tyr)
c.11650C>T (p.His3884Tyr)
16g.88439205A=CA2241074431ZNF469c.11735A= (p.His3912=)
c.11651A= (p.His3884=)
16g.88439205A>CCA286388464ZNF469c.11735A>C (p.His3912Pro)
c.11651A>C (p.His3884Pro)
dbSNP gnomAD v4
16g.88439205A>GCA397131120ZNF469c.11735A>G (p.His3912Arg)
c.11651A>G (p.His3884Arg)
16g.88439205A>TCA397131121ZNF469c.11735A>T (p.His3912Leu)
c.11651A>T (p.His3884Leu)
16g.88439206C>ACA397131123ZNF469c.11736C>A (p.His3912Gln)
c.11652C>A (p.His3884Gln)
dbSNP gnomAD v3 gnomAD v4
16g.88439206C=CA2241074435ZNF469c.11736C= (p.His3912=)
c.11652C= (p.His3884=)
16g.88439206C>GCA397131124ZNF469c.11736C>G (p.His3912Gln)
c.11652C>G (p.His3884Gln)
16g.88439206C>TCA497359680ZNF469c.11736C>T (p.His3912=)
c.11652C>T (p.His3884=)
ClinVar dbSNP gnomAD v4
16g.88439207G>ACA286388478ZNF469c.11737G>A (p.Gly3913Ser)
c.11653G>A (p.Gly3885Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439207G>CCA397131126ZNF469c.11737G>C (p.Gly3913Arg)
c.11653G>C (p.Gly3885Arg)
gnomAD v4
16g.88439207G=CA2241074436ZNF469c.11737G= (p.Gly3913=)
c.11653G= (p.Gly3885=)
16g.88439207G>TCA397131128ZNF469c.11737G>T (p.Gly3913Cys)
c.11653G>T (p.Gly3885Cys)
16g.88439208G>ACA397131129ZNF469c.11738G>A (p.Gly3913Asp)
c.11654G>A (p.Gly3885Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439208G>CCA397131132ZNF469c.11738G>C (p.Gly3913Ala)
c.11654G>C (p.Gly3885Ala)
16g.88439208G=CA2241074439ZNF469c.11738G= (p.Gly3913=)
c.11654G= (p.Gly3885=)
16g.88439208G>TCA397131131ZNF469c.11738G>T (p.Gly3913Val)
c.11654G>T (p.Gly3885Val)
16g.88439209T>ACA497359685ZNF469c.11739T>A (p.Gly3913=)
c.11655T>A (p.Gly3885=)
16g.88439209T>CCA497359688ZNF469c.11739T>C (p.Gly3913=)
c.11655T>C (p.Gly3885=)
16g.88439209T>GCA497359687ZNF469c.11739T>G (p.Gly3913=)
c.11655T>G (p.Gly3885=)
16g.88439210G>ACA397131133ZNF469c.11740G>A (p.Ala3914Thr)
c.11656G>A (p.Ala3886Thr)
16g.88439210G>CCA397131134ZNF469c.11740G>C (p.Ala3914Pro)
c.11656G>C (p.Ala3886Pro)
16g.88439210G>TCA397131136ZNF469c.11740G>T (p.Ala3914Ser)
c.11656G>T (p.Ala3886Ser)
16g.88439211C>ACA397131137ZNF469c.11741C>A (p.Ala3914Asp)
c.11657C>A (p.Ala3886Asp)
16g.88439211C>GCA397131139ZNF469c.11741C>G (p.Ala3914Gly)
c.11657C>G (p.Ala3886Gly)
16g.88439211C>TCA397131141ZNF469c.11741C>T (p.Ala3914Val)
c.11657C>T (p.Ala3886Val)
16g.88439212T>ACA497359693ZNF469c.11742T>A (p.Ala3914=)
c.11658T>A (p.Ala3886=)
16g.88439212T>CCA497359695ZNF469c.11742T>C (p.Ala3914=)
c.11658T>C (p.Ala3886=)
gnomAD v4
16g.88439212T>GCA497359696ZNF469c.11742T>G (p.Ala3914=)
c.11658T>G (p.Ala3886=)
16g.88439213G>ACA397131145ZNF469c.11743G>A (p.Glu3915Lys)
c.11659G>A (p.Glu3887Lys)
gnomAD v4
16g.88439213G>CCA397131142ZNF469c.11743G>C (p.Glu3915Gln)
c.11659G>C (p.Glu3887Gln)
gnomAD v4
16g.88439213G>TCA397131143ZNF469c.11743G>T (p.Glu3915Ter)
c.11659G>T (p.Glu3887Ter)
gnomAD v4
16g.88439214A>CCA397131146ZNF469c.11744A>C (p.Glu3915Ala)
c.11660A>C (p.Glu3887Ala)
16g.88439214A>GCA397131148ZNF469c.11744A>G (p.Glu3915Gly)
c.11660A>G (p.Glu3887Gly)
16g.88439214A>TCA397131150ZNF469c.11744A>T (p.Glu3915Val)
c.11660A>T (p.Glu3887Val)
16g.88439215delCA2808056666ZNF469c.11745del (p.Glu3915AspfsTer26)
c.11661del (p.Glu3887AspfsTer26)
16g.88439215A=CA2241074442ZNF469c.11745A= (p.Glu3915=)
c.11661A= (p.Glu3887=)
16g.88439215A>CCA8225636ZNF469c.11745A>C (p.Glu3915Asp)
c.11661A>C (p.Glu3887Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.88439215A>GCA497359697ZNF469c.11745A>G (p.Glu3915=)
c.11661A>G (p.Glu3887=)
16g.88439215A>TCA397131152ZNF469c.11745A>T (p.Glu3915Asp)
c.11661A>T (p.Glu3887Asp)
16g.88439216C>ACA397131154ZNF469c.11746C>A (p.Pro3916Thr)
c.11662C>A (p.Pro3888Thr)
16g.88439216C=CA2241074446ZNF469c.11746C= (p.Pro3916=)
c.11662C= (p.Pro3888=)
16g.88439216C>GCA397131157ZNF469c.11746C>G (p.Pro3916Ala)
c.11662C>G (p.Pro3888Ala)
dbSNP gnomAD v2 gnomAD v4
16g.88439216C>TCA397131156ZNF469c.11746C>T (p.Pro3916Ser)
c.11662C>T (p.Pro3888Ser)
16g.88439217delCA2533017979ZNF469c.11747del (p.Pro3916LeufsTer25)
c.11663del (p.Pro3888LeufsTer25)
16g.88439217C>ACA397131158ZNF469c.11747C>A (p.Pro3916His)
c.11663C>A (p.Pro3888His)
16g.88439217C>GCA397131160ZNF469c.11747C>G (p.Pro3916Arg)
c.11663C>G (p.Pro3888Arg)
gnomAD v4
16g.88439217C>TCA397131161ZNF469c.11747C>T (p.Pro3916Leu)
c.11663C>T (p.Pro3888Leu)
16g.88439218T>ACA497359701ZNF469c.11748T>A (p.Pro3916=)
c.11664T>A (p.Pro3888=)
16g.88439218T>CCA497359703ZNF469c.11748T>C (p.Pro3916=)
c.11664T>C (p.Pro3888=)
gnomAD v4
16g.88439218T>GCA497359705ZNF469c.11748T>G (p.Pro3916=)
c.11664T>G (p.Pro3888=)
16g.88439219G>ACA397131163ZNF469c.11749G>A (p.Ala3917Thr)
c.11665G>A (p.Ala3889Thr)
gnomAD v4
16g.88439219G>CCA397131164ZNF469c.11749G>C (p.Ala3917Pro)
c.11665G>C (p.Ala3889Pro)
16g.88439219G>TCA397131166ZNF469c.11749G>T (p.Ala3917Ser)
c.11665G>T (p.Ala3889Ser)
16g.88439220C>ACA397131167ZNF469c.11750C>A (p.Ala3917Asp)
c.11666C>A (p.Ala3889Asp)
gnomAD v4
16g.88439220C=CA2241074450ZNF469c.11750C= (p.Ala3917=)
c.11666C= (p.Ala3889=)
16g.88439220C>GCA397131169ZNF469c.11750C>G (p.Ala3917Gly)
c.11666C>G (p.Ala3889Gly)
16g.88439220C>TCA397131171ZNF469c.11750C>T (p.Ala3917Val)
c.11666C>T (p.Ala3889Val)
dbSNP gnomAD v2 gnomAD v4
16g.88439220_88439223delCA2506693104ZNF469c.11750_11753del (p.Ala3917GlyfsTer23)
c.11666_11669del (p.Ala3889GlyfsTer23)
16g.88439221C>ACA8225637ZNF469c.11751C>A (p.Ala3917=)
c.11667C>A (p.Ala3889=)
dbSNP ExAC
16g.88439221C=CA2241074453ZNF469c.11751C= (p.Ala3917=)
c.11667C= (p.Ala3889=)
16g.88439221C>GCA286388503ZNF469c.11751C>G (p.Ala3917=)
c.11667C>G (p.Ala3889=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439221C>TCA286388508ZNF469c.11751C>T (p.Ala3917=)
c.11667C>T (p.Ala3889=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.88439222G>ACA397131173ZNF469c.11752G>A (p.Glu3918Lys)
c.11668G>A (p.Glu3890Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439222G>CCA397131177ZNF469c.11752G>C (p.Glu3918Gln)
c.11668G>C (p.Glu3890Gln)
16g.88439222G=CA2241074457ZNF469c.11752G= (p.Glu3918=)
c.11668G= (p.Glu3890=)
16g.88439222G>TCA397131175ZNF469c.11752G>T (p.Glu3918Ter)
c.11668G>T (p.Glu3890Ter)
16g.88439223A>CCA397131179ZNF469c.11753A>C (p.Glu3918Ala)
c.11669A>C (p.Glu3890Ala)
16g.88439223A>GCA397131182ZNF469c.11753A>G (p.Glu3918Gly)
c.11669A>G (p.Glu3890Gly)
16g.88439223A>TCA397131180ZNF469c.11753A>T (p.Glu3918Val)
c.11669A>T (p.Glu3890Val)
16g.88439224G>ACA497359711ZNF469c.11754G>A (p.Glu3918=)
c.11670G>A (p.Glu3890=)
gnomAD v4
16g.88439224G>CCA397131184ZNF469c.11754G>C (p.Glu3918Asp)
c.11670G>C (p.Glu3890Asp)
16g.88439224G>TCA397131186ZNF469c.11754G>T (p.Glu3918Asp)
c.11670G>T (p.Glu3890Asp)
16g.88439225C>ACA397131187ZNF469c.11755C>A (p.Pro3919Thr)
c.11671C>A (p.Pro3891Thr)
16g.88439225C>GCA397131188ZNF469c.11755C>G (p.Pro3919Ala)
c.11671C>G (p.Pro3891Ala)
16g.88439225C>TCA397131190ZNF469c.11755C>T (p.Pro3919Ser)
c.11671C>T (p.Pro3891Ser)
gnomAD v4
16g.88439226C>ACA397131192ZNF469c.11756C>A (p.Pro3919Gln)
c.11672C>A (p.Pro3891Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439226C=CA2241074460ZNF469c.11756C= (p.Pro3919=)
c.11672C= (p.Pro3891=)
16g.88439226C>GCA397131194ZNF469c.11756C>G (p.Pro3919Arg)
c.11672C>G (p.Pro3891Arg)
16g.88439226C>TCA8225638ZNF469c.11756C>T (p.Pro3919Leu)
c.11672C>T (p.Pro3891Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439226_88439227delinsTGCA2580092243ZNF469c.11756_11757delinsTG (p.Pro3919Leu)
c.11672_11673delinsTG (p.Pro3891Leu)
ClinVar
16g.88439227A=CA2241074465ZNF469c.11757A= (p.Pro3919=)
c.11673A= (p.Pro3891=)
16g.88439227A>CCA497359712ZNF469c.11757A>C (p.Pro3919=)
c.11673A>C (p.Pro3891=)
16g.88439227A>GCA8225639ZNF469c.11757A>G (p.Pro3919=)
c.11673A>G (p.Pro3891=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439227A>TCA497359714ZNF469c.11757A>T (p.Pro3919=)
c.11673A>T (p.Pro3891=)
gnomAD v4
16g.88439228C>ACA397131198ZNF469c.11758C>A (p.His3920Asn)
c.11674C>A (p.His3892Asn)
16g.88439228C>GCA397131199ZNF469c.11758C>G (p.His3920Asp)
c.11674C>G (p.His3892Asp)
16g.88439228C>TCA397131200ZNF469c.11758C>T (p.His3920Tyr)
c.11674C>T (p.His3892Tyr)
gnomAD v4
16g.88439229delCA2559288839ZNF469c.11759del (p.His3920ProfsTer21)
c.11675del (p.His3892ProfsTer21)
16g.88439229A=CA2241074467ZNF469c.11759A= (p.His3920=)
c.11675A= (p.His3892=)
16g.88439229A>CCA397131201ZNF469c.11759A>C (p.His3920Pro)
c.11675A>C (p.His3892Pro)
16g.88439229A>GCA397131202ZNF469c.11759A>G (p.His3920Arg)
c.11675A>G (p.His3892Arg)
16g.88439229A>TCA8225640ZNF469c.11759A>T (p.His3920Leu)
c.11675A>T (p.His3892Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439230C>ACA397131203ZNF469c.11760C>A (p.His3920Gln)
c.11676C>A (p.His3892Gln)
gnomAD v4
16g.88439230C>GCA397131204ZNF469c.11760C>G (p.His3920Gln)
c.11676C>G (p.His3892Gln)
16g.88439230C>TCA497359716ZNF469c.11760C>T (p.His3920=)
c.11676C>T (p.His3892=)
gnomAD v4
16g.88439231A=CA2241074470ZNF469c.11761A= (p.Thr3921=)
c.11677A= (p.Thr3893=)
16g.88439231A>CCA397131205ZNF469c.11761A>C (p.Thr3921Pro)
c.11677A>C (p.Thr3893Pro)
16g.88439231A>GCA397131206ZNF469c.11761A>G (p.Thr3921Ala)
c.11677A>G (p.Thr3893Ala)
16g.88439231A>TCA397131207ZNF469c.11761A>T (p.Thr3921Ser)
c.11677A>T (p.Thr3893Ser)
16g.88439232C>ACA397131208ZNF469c.11762C>A (p.Thr3921Asn)
c.11678C>A (p.Thr3893Asn)
gnomAD v4
16g.88439232C>GCA397131209ZNF469c.11762C>G (p.Thr3921Ser)
c.11678C>G (p.Thr3893Ser)
16g.88439232C>TCA397131210ZNF469c.11762C>T (p.Thr3921Ile)
c.11678C>T (p.Thr3893Ile)
gnomAD v4
16g.88439232_88439237dupCA8225641ZNF469c.11762_11767dup (p.His3922_Arg3923insProHis)
c.11678_11683dup (p.His3894_Arg3895insProHis)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.88439233C>ACA497359719ZNF469c.11763C>A (p.Thr3921=)
c.11679C>A (p.Thr3893=)
16g.88439233C>GCA497359720ZNF469c.11763C>G (p.Thr3921=)
c.11679C>G (p.Thr3893=)
ClinVar
16g.88439233C>TCA497359721ZNF469c.11763C>T (p.Thr3921=)
c.11679C>T (p.Thr3893=)
16g.88439234C>ACA397131213ZNF469c.11764C>A (p.His3922Asn)
c.11680C>A (p.His3894Asn)
gnomAD v4
16g.88439234C=CA2241074475ZNF469c.11764C= (p.His3922=)
c.11680C= (p.His3894=)
16g.88439234C>GCA397131212ZNF469c.11764C>G (p.His3922Asp)
c.11680C>G (p.His3894Asp)
16g.88439234C>TCA397131211ZNF469c.11764C>T (p.His3922Tyr)
c.11680C>T (p.His3894Tyr)
dbSNP gnomAD v2 gnomAD v4
16g.88439234_88439235insGGCA2531214747ZNF469c.11764_11765insGG (p.His3922ArgfsTer20)
c.11680_11681insGG (p.His3894ArgfsTer20)
16g.88439235A>CCA397131214ZNF469c.11765A>C (p.His3922Pro)
c.11681A>C (p.His3894Pro)
16g.88439235A>GCA397131215ZNF469c.11765A>G (p.His3922Arg)
c.11681A>G (p.His3894Arg)
16g.88439235A>TCA397131216ZNF469c.11765A>T (p.His3922Leu)
c.11681A>T (p.His3894Leu)
16g.88439236C>ACA286388523ZNF469c.11766C>A (p.His3922Gln)
c.11682C>A (p.His3894Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439236C=CA2241074478ZNF469c.11766C= (p.His3922=)
c.11682C= (p.His3894=)
16g.88439236C>GCA397131217ZNF469c.11766C>G (p.His3922Gln)
c.11682C>G (p.His3894Gln)
dbSNP gnomAD v2 gnomAD v4
16g.88439236C>TCA497359727ZNF469c.11766C>T (p.His3922=)
c.11682C>T (p.His3894=)
gnomAD v4
16g.88439237C>ACA497359728ZNF469c.11767C>A (p.Arg3923=)
c.11683C>A (p.Arg3895=)
gnomAD v4
16g.88439237C=CA2241074480ZNF469c.11767C= (p.Arg3923=)
c.11683C= (p.Arg3895=)
16g.88439237C>GCA397131218ZNF469c.11767C>G (p.Arg3923Gly)
c.11683C>G (p.Arg3895Gly)
gnomAD v4
16g.88439237C>TCA286388526ZNF469c.11767C>T (p.Arg3923Trp)
c.11683C>T (p.Arg3895Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439237_88439238insTGCACA2529139807ZNF469c.11767_11768insTGCA (p.Arg3923LeufsTer9)
c.11683_11684insTGCA (p.Arg3895LeufsTer9)
16g.88439238G>ACA286388537ZNF469c.11768G>A (p.Arg3923Gln)
c.11684G>A (p.Arg3895Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439238G>CCA286388531ZNF469c.11768G>C (p.Arg3923Pro)
c.11684G>C (p.Arg3895Pro)
dbSNP
16g.88439238G=CA2241074483ZNF469c.11768G= (p.Arg3923=)
c.11684G= (p.Arg3895=)
16g.88439238G>TCA397131219ZNF469c.11768G>T (p.Arg3923Leu)
c.11684G>T (p.Arg3895Leu)
16g.88439239delCA2808056675ZNF469c.11769del (p.Thr3924ArgfsTer17)
c.11685del (p.Thr3896ArgfsTer17)
16g.88439239G>ACA497359730ZNF469c.11769G>A (p.Arg3923=)
c.11685G>A (p.Arg3895=)
gnomAD v4
16g.88439239G>CCA497359732ZNF469c.11769G>C (p.Arg3923=)
c.11685G>C (p.Arg3895=)
16g.88439239G>TCA497359733ZNF469c.11769G>T (p.Arg3923=)
c.11685G>T (p.Arg3895=)
ClinVar gnomAD v4
16g.88439240A>CCA397131220ZNF469c.11770A>C (p.Thr3924Pro)
c.11686A>C (p.Thr3896Pro)
16g.88439240A>GCA397131221ZNF469c.11770A>G (p.Thr3924Ala)
c.11686A>G (p.Thr3896Ala)
16g.88439240A>TCA397131222ZNF469c.11770A>T (p.Thr3924Ser)
c.11686A>T (p.Thr3896Ser)
16g.88439241C>ACA397131223ZNF469c.11771C>A (p.Thr3924Lys)
c.11687C>A (p.Thr3896Lys)
dbSNP
16g.88439241C=CA2241074488ZNF469c.11771C= (p.Thr3924=)
c.11687C= (p.Thr3896=)
16g.88439241C>GCA286388538ZNF469c.11771C>G (p.Thr3924Arg)
c.11687C>G (p.Thr3896Arg)
dbSNP
16g.88439241C>TCA8225642ZNF469c.11771C>T (p.Thr3924Met)
c.11687C>T (p.Thr3896Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439242G>ACA8225643ZNF469c.11772G>A (p.Thr3924=)
c.11688G>A (p.Thr3896=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439242G>CCA497359735ZNF469c.11772G>C (p.Thr3924=)
c.11688G>C (p.Thr3896=)
16g.88439242G=CA2241074490ZNF469c.11772G= (p.Thr3924=)
c.11688G= (p.Thr3896=)
16g.88439242G>TCA497359737ZNF469c.11772G>T (p.Thr3924=)
c.11688G>T (p.Thr3896=)
16g.88439243G>ACA397131224ZNF469c.11773G>A (p.Ala3925Thr)
c.11689G>A (p.Ala3897Thr)
gnomAD v4
16g.88439243G>CCA397131225ZNF469c.11773G>C (p.Ala3925Pro)
c.11689G>C (p.Ala3897Pro)
16g.88439243G>TCA397131226ZNF469c.11773G>T (p.Ala3925Ser)
c.11689G>T (p.Ala3897Ser)
16g.88439243_88439244delinsGCCA2241074491ZNF469c.11773_11774delinsGC (p.Ala3925=)
c.11689_11690delinsGC (p.Ala3897=)
16g.88439244C>ACA397131227ZNF469c.11774C>A (p.Ala3925Asp)
c.11690C>A (p.Ala3897Asp)
16g.88439244C=CA2241074494ZNF469c.11774C= (p.Ala3925=)
c.11690C= (p.Ala3897=)
16g.88439244C>GCA397131228ZNF469c.11774C>G (p.Ala3925Gly)
c.11690C>G (p.Ala3897Gly)
16g.88439244C>TCA397131229ZNF469c.11774C>T (p.Ala3925Val)
c.11690C>T (p.Ala3897Val)
dbSNP gnomAD v2 gnomAD v4
16g.88439245delCA980292090ZNF469c.11775del (p.Glu3926ArgfsTer15)
c.11691del (p.Glu3898ArgfsTer15)
dbSNP gnomAD v3 gnomAD v4
16g.88439245C>ACA497359740ZNF469c.11775C>A (p.Ala3925=)
c.11691C>A (p.Ala3897=)
dbSNP gnomAD v2 gnomAD v4
16g.88439245C=CA2241074499ZNF469c.11775C= (p.Ala3925=)
c.11691C= (p.Ala3897=)
16g.88439245C>GCA8225644ZNF469c.11775C>G (p.Ala3925=)
c.11691C>G (p.Ala3897=)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.88439245C>TCA497359743ZNF469c.11775C>T (p.Ala3925=)
c.11691C>T (p.Ala3897=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439245_88439248delinsCGAGCA2241074502ZNF469c.11775_11778delinsCGAG (p.Ala3925=)
c.11691_11694delinsCGAG (p.Ala3897=)
16g.88439246G>ACA8225646ZNF469c.11776G>A (p.Glu3926Lys)
c.11692G>A (p.Glu3898Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.88439246G>CCA397131230ZNF469c.11776G>C (p.Glu3926Gln)
c.11692G>C (p.Glu3898Gln)
16g.88439246G=CA2241074504ZNF469c.11776G= (p.Glu3926=)
c.11692G= (p.Glu3898=)
16g.88439246G>TCA397131231ZNF469c.11776G>T (p.Glu3926Ter)
c.11692G>T (p.Glu3898Ter)
16g.88439247_88439249delCA8225645ZNF469c.11777_11779del (p.Glu3926del)
c.11693_11695del (p.Glu3898del)
dbSNP ExAC
16g.88439247A>CCA397131233ZNF469c.11777A>C (p.Glu3926Ala)
c.11693A>C (p.Glu3898Ala)
16g.88439247A>GCA397131234ZNF469c.11777A>G (p.Glu3926Gly)
c.11693A>G (p.Glu3898Gly)
gnomAD v4
16g.88439247A>TCA397131232ZNF469c.11777A>T (p.Glu3926Val)
c.11693A>T (p.Glu3898Val)
16g.88439248G>ACA497359745ZNF469c.11778G>A (p.Glu3926=)
c.11694G>A (p.Glu3898=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439248G>CCA397131236ZNF469c.11778G>C (p.Glu3926Asp)
c.11694G>C (p.Glu3898Asp)
16g.88439248G=CA2241074507ZNF469c.11778G= (p.Glu3926=)
c.11694G= (p.Glu3898=)
16g.88439248G>TCA397131235ZNF469c.11778G>T (p.Glu3926Asp)
c.11694G>T (p.Glu3898Asp)
16g.88439249G>ACA397131239ZNF469c.11779G>A (p.Ala3927Thr)
c.11695G>A (p.Ala3899Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439249G>CCA397131237ZNF469c.11779G>C (p.Ala3927Pro)
c.11695G>C (p.Ala3899Pro)
16g.88439249G=CA2241074512ZNF469c.11779G= (p.Ala3927=)
c.11695G= (p.Ala3899=)
16g.88439249G>TCA397131238ZNF469c.11779G>T (p.Ala3927Ser)
c.11695G>T (p.Ala3899Ser)
dbSNP gnomAD v2
16g.88439250C>ACA397131240ZNF469c.11780C>A (p.Ala3927Asp)
c.11696C>A (p.Ala3899Asp)
16g.88439250C=CA2241074514ZNF469c.11780C= (p.Ala3927=)
c.11696C= (p.Ala3899=)
16g.88439250C>GCA397131241ZNF469c.11780C>G (p.Ala3927Gly)
c.11696C>G (p.Ala3899Gly)
16g.88439250C>TCA397131242ZNF469c.11780C>T (p.Ala3927Val)
c.11696C>T (p.Ala3899Val)
gnomAD v4
16g.88439252delCA2808056680ZNF469c.11782del (p.Gln3928ArgfsTer13)
c.11698del (p.Gln3900ArgfsTer13)
16g.88439250_88439251insACACCCACA8225647ZNF469c.11780_11781insACACCCA (p.Gln3928HisfsTer5)
c.11696_11697insACACCCA (p.Gln3900HisfsTer5)
dbSNP ExAC
16g.88439251C>ACA497359750ZNF469c.11781C>A (p.Ala3927=)
c.11697C>A (p.Ala3899=)
16g.88439251C>GCA497359751ZNF469c.11781C>G (p.Ala3927=)
c.11697C>G (p.Ala3899=)
ClinVar
16g.88439251C>TCA497359752ZNF469c.11781C>T (p.Ala3927=)
c.11697C>T (p.Ala3899=)
16g.88439252C>ACA397131245ZNF469c.11782C>A (p.Gln3928Lys)
c.11698C>A (p.Gln3900Lys)
16g.88439252C>GCA397131243ZNF469c.11782C>G (p.Gln3928Glu)
c.11698C>G (p.Gln3900Glu)
16g.88439252C>TCA397131244ZNF469c.11782C>T (p.Gln3928Ter)
c.11698C>T (p.Gln3900Ter)
16g.88439253A=CA2241074517ZNF469c.11783A= (p.Gln3928=)
c.11699A= (p.Gln3900=)
16g.88439253A>CCA397131246ZNF469c.11783A>C (p.Gln3928Pro)
c.11699A>C (p.Gln3900Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439253A>GCA397131247ZNF469c.11783A>G (p.Gln3928Arg)
c.11699A>G (p.Gln3900Arg)
16g.88439253A>TCA286388563ZNF469c.11783A>T (p.Gln3928Leu)
c.11699A>T (p.Gln3900Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439255_88439256delCA2576089666ZNF469c.11785_11786del (p.Ser3929Ter)
c.11701_11702del (p.Ser3901Ter)
16g.88439254G>ACA497359760ZNF469c.11784G>A (p.Gln3928=)
c.11700G>A (p.Gln3900=)
dbSNP
16g.88439254G>CCA397131248ZNF469c.11784G>C (p.Gln3928His)
c.11700G>C (p.Gln3900His)
gnomAD v4
16g.88439254G=CA2241074520ZNF469c.11784G= (p.Gln3928=)
c.11700G= (p.Gln3900=)
16g.88439254G>TCA397131249ZNF469c.11784G>T (p.Gln3928His)
c.11700G>T (p.Gln3900His)
16g.88439255A=CA2241074523ZNF469c.11785A= (p.Ser3929=)
c.11701A= (p.Ser3901=)
16g.88439255A>CCA397131250ZNF469c.11785A>C (p.Ser3929Arg)
c.11701A>C (p.Ser3901Arg)
16g.88439255A>GCA397131252ZNF469c.11785A>G (p.Ser3929Gly)
c.11701A>G (p.Ser3901Gly)
dbSNP gnomAD v3 gnomAD v4
16g.88439255A>TCA397131251ZNF469c.11785A>T (p.Ser3929Cys)
c.11701A>T (p.Ser3901Cys)
16g.88439256G>ACA397131253ZNF469c.11786G>A (p.Ser3929Asn)
c.11702G>A (p.Ser3901Asn)
16g.88439256G>CCA397131254ZNF469c.11786G>C (p.Ser3929Thr)
c.11702G>C (p.Ser3901Thr)
dbSNP gnomAD v2 gnomAD v4
16g.88439256G=CA2241074524ZNF469c.11786G= (p.Ser3929=)
c.11702G= (p.Ser3901=)
16g.88439256G>TCA397131255ZNF469c.11786G>T (p.Ser3929Ile)
c.11702G>T (p.Ser3901Ile)
16g.88439257T>ACA397131256ZNF469c.11787T>A (p.Ser3929Arg)
c.11703T>A (p.Ser3901Arg)
16g.88439257T>CCA497359763ZNF469c.11787T>C (p.Ser3929=)
c.11703T>C (p.Ser3901=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439257T>GCA397131257ZNF469c.11787T>G (p.Ser3929Arg)
c.11703T>G (p.Ser3901Arg)
16g.88439257T=CA2241074525ZNF469c.11787T= (p.Ser3929=)
c.11703T= (p.Ser3901=)
16g.88439258G>ACA397131258ZNF469c.11788G>A (p.Asp3930Asn)
c.11704G>A (p.Asp3902Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439258G>CCA397131259ZNF469c.11788G>C (p.Asp3930His)
c.11704G>C (p.Asp3902His)
16g.88439258G=CA2241074527ZNF469c.11788G= (p.Asp3930=)
c.11704G= (p.Asp3902=)
16g.88439258G>TCA397131260ZNF469c.11788G>T (p.Asp3930Tyr)
c.11704G>T (p.Asp3902Tyr)
16g.88439259A=CA2241074529ZNF469c.11789A= (p.Asp3930=)
c.11705A= (p.Asp3902=)
16g.88439259A>CCA397131261ZNF469c.11789A>C (p.Asp3930Ala)
c.11705A>C (p.Asp3902Ala)
16g.88439259A>GCA397131262ZNF469c.11789A>G (p.Asp3930Gly)
c.11705A>G (p.Asp3902Gly)
dbSNP
16g.88439259A>TCA397131263ZNF469c.11789A>T (p.Asp3930Val)
c.11705A>T (p.Asp3902Val)
16g.88439260C>ACA397131264ZNF469c.11790C>A (p.Asp3930Glu)
c.11706C>A (p.Asp3902Glu)
16g.88439260C>GCA397131265ZNF469c.11790C>G (p.Asp3930Glu)
c.11706C>G (p.Asp3902Glu)
16g.88439260C>TCA497359769ZNF469c.11790C>T (p.Asp3930=)
c.11706C>T (p.Asp3902=)
16g.88439261C>ACA397131266ZNF469c.11791C>A (p.Leu3931Ile)
c.11707C>A (p.Leu3903Ile)
16g.88439261C=CA2241074534ZNF469c.11791C= (p.Leu3931=)
c.11707C= (p.Leu3903=)
16g.88439261C>GCA397131267ZNF469c.11791C>G (p.Leu3931Val)
c.11707C>G (p.Leu3903Val)
gnomAD v4
16g.88439261C>TCA397131268ZNF469c.11791C>T (p.Leu3931Phe)
c.11707C>T (p.Leu3903Phe)
dbSNP gnomAD v2 gnomAD v4
16g.88439262T>ACA397131269ZNF469c.11792T>A (p.Leu3931His)
c.11708T>A (p.Leu3903His)
gnomAD v4
16g.88439262T>CCA397131270ZNF469c.11792T>C (p.Leu3931Pro)
c.11708T>C (p.Leu3903Pro)
gnomAD v4
16g.88439262T>GCA397131271ZNF469c.11792T>G (p.Leu3931Arg)
c.11708T>G (p.Leu3903Arg)
16g.88439263C>ACA497359774ZNF469c.11793C>A (p.Leu3931=)
c.11709C>A (p.Leu3903=)
16g.88439263C>GCA497359776ZNF469c.11793C>G (p.Leu3931=)
c.11709C>G (p.Leu3903=)
16g.88439263C>TCA497359778ZNF469c.11793C>T (p.Leu3931=)
c.11709C>T (p.Leu3903=)
gnomAD v4
16g.88439264C>ACA397131272ZNF469c.11794C>A (p.Leu3932Ile)
c.11710C>A (p.Leu3904Ile)
16g.88439264C>GCA397131273ZNF469c.11794C>G (p.Leu3932Val)
c.11710C>G (p.Leu3904Val)
16g.88439264C>TCA397131274ZNF469c.11794C>T (p.Leu3932Phe)
c.11710C>T (p.Leu3904Phe)
16g.88439265T>ACA397131275ZNF469c.11795T>A (p.Leu3932His)
c.11711T>A (p.Leu3904His)
16g.88439265T>CCA397131276ZNF469c.11795T>C (p.Leu3932Pro)
c.11711T>C (p.Leu3904Pro)
16g.88439265T>GCA397131277ZNF469c.11795T>G (p.Leu3932Arg)
c.11711T>G (p.Leu3904Arg)
16g.88439266C>ACA497359786ZNF469c.11796C>A (p.Leu3932=)
c.11712C>A (p.Leu3904=)
16g.88439266C>GCA497359785ZNF469c.11796C>G (p.Leu3932=)
c.11712C>G (p.Leu3904=)
16g.88439266C>TCA497359783ZNF469c.11796C>T (p.Leu3932=)
c.11712C>T (p.Leu3904=)
16g.88439267A=CA2241074537ZNF469c.11797A= (p.Ser3933=)
c.11713A= (p.Ser3905=)
16g.88439267A>CCA397131279ZNF469c.11797A>C (p.Ser3933Arg)
c.11713A>C (p.Ser3905Arg)
16g.88439267A>GCA397131280ZNF469c.11797A>G (p.Ser3933Gly)
c.11713A>G (p.Ser3905Gly)
dbSNP gnomAD v4
16g.88439267A>TCA397131278ZNF469c.11797A>T (p.Ser3933Cys)
c.11713A>T (p.Ser3905Cys)
16g.88439268G>ACA397131281ZNF469c.11798G>A (p.Ser3933Asn)
c.11714G>A (p.Ser3905Asn)
dbSNP
16g.88439268G>CCA397131282ZNF469c.11798G>C (p.Ser3933Thr)
c.11714G>C (p.Ser3905Thr)
16g.88439268G=CA2241074539ZNF469c.11798G= (p.Ser3933=)
c.11714G= (p.Ser3905=)
16g.88439268G>TCA397131283ZNF469c.11798G>T (p.Ser3933Ile)
c.11714G>T (p.Ser3905Ile)
16g.88439269_88439280delCA2634824444ZNF469c.11799_11810del (p.Ser3933_Gly3937delinsArg)
c.11715_11726del (p.Ser3905_Gly3909delinsArg)
gnomAD v4
16g.88439269C>ACA397131284ZNF469c.11799C>A (p.Ser3933Arg)
c.11715C>A (p.Ser3905Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439269C=CA2241074540ZNF469c.11799C= (p.Ser3933=)
c.11715C= (p.Ser3905=)
16g.88439269C>GCA397131285ZNF469c.11799C>G (p.Ser3933Arg)
c.11715C>G (p.Ser3905Arg)
16g.88439269C>TCA497359792ZNF469c.11799C>T (p.Ser3933=)
c.11715C>T (p.Ser3905=)

Number of alleles fetched