Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.88437440C>ACA397125341ZNF469c.9970C>A (p.Gln3324Lys)
c.9886C>A (p.Gln3296Lys)
gnomAD v4
16g.88437440C=CA2241073091ZNF469c.9970C= (p.Gln3324=)
c.9886C= (p.Gln3296=)
16g.88437440C>GCA286386039ZNF469c.9970C>G (p.Gln3324Glu)
c.9886C>G (p.Gln3296Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437440C>TCA397125344ZNF469c.9970C>T (p.Gln3324Ter)
c.9886C>T (p.Gln3296Ter)
16g.88437441A=CA2241073093ZNF469c.9971A= (p.Gln3324=)
c.9887A= (p.Gln3296=)
16g.88437441A>CCA397125347ZNF469c.9971A>C (p.Gln3324Pro)
c.9887A>C (p.Gln3296Pro)
16g.88437441A>GCA397125345ZNF469c.9971A>G (p.Gln3324Arg)
c.9887A>G (p.Gln3296Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437441A>TCA397125346ZNF469c.9971A>T (p.Gln3324Leu)
c.9887A>T (p.Gln3296Leu)
16g.88437442A>CCA397125348ZNF469c.9972A>C (p.Gln3324His)
c.9888A>C (p.Gln3296His)
16g.88437442A>GCA497358577ZNF469c.9972A>G (p.Gln3324=)
c.9888A>G (p.Gln3296=)
16g.88437442A>TCA397125349ZNF469c.9972A>T (p.Gln3324His)
c.9888A>T (p.Gln3296His)
16g.88437443G>ACA397125350ZNF469c.9973G>A (p.Ala3325Thr)
c.9889G>A (p.Ala3297Thr)
16g.88437443G>CCA397125351ZNF469c.9973G>C (p.Ala3325Pro)
c.9889G>C (p.Ala3297Pro)
16g.88437443G=CA2241073094ZNF469c.9973G= (p.Ala3325=)
c.9889G= (p.Ala3297=)
16g.88437443G>TCA397125352ZNF469c.9973G>T (p.Ala3325Ser)
c.9889G>T (p.Ala3297Ser)
dbSNP gnomAD v2
16g.88437445_88437466delCA2634824447ZNF469c.9975_9996del (p.Thr3326ArgfsTer?)
c.9891_9912del (p.Thr3298ArgfsTer?)
gnomAD v4
16g.88437444C>ACA397125353ZNF469c.9974C>A (p.Ala3325Asp)
c.9890C>A (p.Ala3297Asp)
16g.88437444C>GCA397125355ZNF469c.9974C>G (p.Ala3325Gly)
c.9890C>G (p.Ala3297Gly)
16g.88437444C>TCA397125354ZNF469c.9974C>T (p.Ala3325Val)
c.9890C>T (p.Ala3297Val)
gnomAD v4
16g.88437445C>ACA497358578ZNF469c.9975C>A (p.Ala3325=)
c.9891C>A (p.Ala3297=)
gnomAD v4
16g.88437445C>GCA497358579ZNF469c.9975C>G (p.Ala3325=)
c.9891C>G (p.Ala3297=)
16g.88437445C>TCA497358580ZNF469c.9975C>T (p.Ala3325=)
c.9891C>T (p.Ala3297=)
16g.88437446A=CA2241073096ZNF469c.9976A= (p.Thr3326=)
c.9892A= (p.Thr3298=)
16g.88437446A>CCA397125356ZNF469c.9976A>C (p.Thr3326Pro)
c.9892A>C (p.Thr3298Pro)
gnomAD v4
16g.88437446A>GCA397125357ZNF469c.9976A>G (p.Thr3326Ala)
c.9892A>G (p.Thr3298Ala)
dbSNP
16g.88437446A>TCA397125358ZNF469c.9976A>T (p.Thr3326Ser)
c.9892A>T (p.Thr3298Ser)
16g.88437447C>ACA397125359ZNF469c.9977C>A (p.Thr3326Asn)
c.9893C>A (p.Thr3298Asn)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88437447C=CA2241073099ZNF469c.9977C= (p.Thr3326=)
c.9893C= (p.Thr3298=)
16g.88437447C>GCA397125360ZNF469c.9977C>G (p.Thr3326Ser)
c.9893C>G (p.Thr3298Ser)
gnomAD v4
16g.88437447C>TCA397125361ZNF469c.9977C>T (p.Thr3326Ile)
c.9893C>T (p.Thr3298Ile)
dbSNP gnomAD v4
16g.88437450delCA2634824448ZNF469c.9980del (p.Pro3327ArgfsTer?)
c.9896del (p.Pro3299ArgfsTer?)
gnomAD v4
16g.88437448C>ACA497358581ZNF469c.9978C>A (p.Thr3326=)
c.9894C>A (p.Thr3298=)
16g.88437448C>GCA497358583ZNF469c.9978C>G (p.Thr3326=)
c.9894C>G (p.Thr3298=)
gnomAD v4 COSMIC
16g.88437448C>TCA497358582ZNF469c.9978C>T (p.Thr3326=)
c.9894C>T (p.Thr3298=)
gnomAD v4
16g.88437449C>ACA397125362ZNF469c.9979C>A (p.Pro3327Thr)
c.9895C>A (p.Pro3299Thr)
gnomAD v4
16g.88437449C>GCA397125363ZNF469c.9979C>G (p.Pro3327Ala)
c.9895C>G (p.Pro3299Ala)
gnomAD v4
16g.88437449C>TCA397125364ZNF469c.9979C>T (p.Pro3327Ser)
c.9895C>T (p.Pro3299Ser)
gnomAD v4
16g.88437450C>ACA397125365ZNF469c.9980C>A (p.Pro3327Gln)
c.9896C>A (p.Pro3299Gln)
16g.88437450C=CA2241073101ZNF469c.9980C= (p.Pro3327=)
c.9896C= (p.Pro3299=)
16g.88437450C>GCA397125366ZNF469c.9980C>G (p.Pro3327Arg)
c.9896C>G (p.Pro3299Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88437450C>TCA286386051ZNF469c.9980C>T (p.Pro3327Leu)
c.9896C>T (p.Pro3299Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437451G>ACA497358584ZNF469c.9981G>A (p.Pro3327=)
c.9897G>A (p.Pro3299=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88437451G>CCA497358585ZNF469c.9981G>C (p.Pro3327=)
c.9897G>C (p.Pro3299=)
gnomAD v4
16g.88437451G=CA2241073102ZNF469c.9981G= (p.Pro3327=)
c.9897G= (p.Pro3299=)
16g.88437451G>TCA497358586ZNF469c.9981G>T (p.Pro3327=)
c.9897G>T (p.Pro3299=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437452G>ACA397125369ZNF469c.9982G>A (p.Val3328Met)
c.9898G>A (p.Val3300Met)
16g.88437452G>CCA397125368ZNF469c.9982G>C (p.Val3328Leu)
c.9898G>C (p.Val3300Leu)
16g.88437452G=CA2241073103ZNF469c.9982G= (p.Val3328=)
c.9898G= (p.Val3300=)
16g.88437452G>TCA397125367ZNF469c.9982G>T (p.Val3328Leu)
c.9898G>T (p.Val3300Leu)
dbSNP gnomAD v2 gnomAD v4
16g.88437453T>ACA397125370ZNF469c.9983T>A (p.Val3328Glu)
c.9899T>A (p.Val3300Glu)
16g.88437453T>CCA397125371ZNF469c.9983T>C (p.Val3328Ala)
c.9899T>C (p.Val3300Ala)
16g.88437453T>GCA397125372ZNF469c.9983T>G (p.Val3328Gly)
c.9899T>G (p.Val3300Gly)
16g.88437454G>ACA286386057ZNF469c.9984G>A (p.Val3328=)
c.9900G>A (p.Val3300=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437454G>CCA497358587ZNF469c.9984G>C (p.Val3328=)
c.9900G>C (p.Val3300=)
16g.88437454G=CA2241073106ZNF469c.9984G= (p.Val3328=)
c.9900G= (p.Val3300=)
16g.88437454G>TCA497358588ZNF469c.9984G>T (p.Val3328=)
c.9900G>T (p.Val3300=)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88437455C>ACA397125373ZNF469c.9985C>A (p.His3329Asn)
c.9901C>A (p.His3301Asn)
16g.88437455C>GCA397125374ZNF469c.9985C>G (p.His3329Asp)
c.9901C>G (p.His3301Asp)
16g.88437455C>TCA397125375ZNF469c.9985C>T (p.His3329Tyr)
c.9901C>T (p.His3301Tyr)
ClinVar gnomAD v4
16g.88437456A>CCA397125376ZNF469c.9986A>C (p.His3329Pro)
c.9902A>C (p.His3301Pro)
16g.88437456A>GCA397125377ZNF469c.9986A>G (p.His3329Arg)
c.9902A>G (p.His3301Arg)
gnomAD v4
16g.88437456A>TCA397125378ZNF469c.9986A>T (p.His3329Leu)
c.9902A>T (p.His3301Leu)
gnomAD v4
16g.88437457C>ACA397125379ZNF469c.9987C>A (p.His3329Gln)
c.9903C>A (p.His3301Gln)
gnomAD v4
16g.88437457C=CA2241073107ZNF469c.9987C= (p.His3329=)
c.9903C= (p.His3301=)
16g.88437457C>GCA397125380ZNF469c.9987C>G (p.His3329Gln)
c.9903C>G (p.His3301Gln)
dbSNP gnomAD v2 gnomAD v4
16g.88437457C>TCA497358589ZNF469c.9987C>T (p.His3329=)
c.9903C>T (p.His3301=)
dbSNP gnomAD v2 gnomAD v4
16g.88437458G>ACA397125381ZNF469c.9988G>A (p.Glu3330Lys)
c.9904G>A (p.Glu3302Lys)
ClinVar dbSNP gnomAD v4
16g.88437458G>CCA397125383ZNF469c.9988G>C (p.Glu3330Gln)
c.9904G>C (p.Glu3302Gln)
gnomAD v4
16g.88437458G=CA2241073109ZNF469c.9988G= (p.Glu3330=)
c.9904G= (p.Glu3302=)
16g.88437458G>TCA397125382ZNF469c.9988G>T (p.Glu3330Ter)
c.9904G>T (p.Glu3302Ter)
16g.88437459A=CA2241073111ZNF469c.9989A= (p.Glu3330=)
c.9905A= (p.Glu3302=)
16g.88437459A>CCA397125384ZNF469c.9989A>C (p.Glu3330Ala)
c.9905A>C (p.Glu3302Ala)
16g.88437459A>GCA397125386ZNF469c.9989A>G (p.Glu3330Gly)
c.9905A>G (p.Glu3302Gly)
gnomAD v4
16g.88437459A>TCA397125385ZNF469c.9989A>T (p.Glu3330Val)
c.9905A>T (p.Glu3302Val)
dbSNP
16g.88437460G>ACA497358590ZNF469c.9990G>A (p.Glu3330=)
c.9906G>A (p.Glu3302=)
gnomAD v4
16g.88437460G>CCA397125387ZNF469c.9990G>C (p.Glu3330Asp)
c.9906G>C (p.Glu3302Asp)
16g.88437460G>TCA397125388ZNF469c.9990G>T (p.Glu3330Asp)
c.9906G>T (p.Glu3302Asp)
16g.88437461G>ACA397125389ZNF469c.9991G>A (p.Ala3331Thr)
c.9907G>A (p.Ala3303Thr)
gnomAD v4
16g.88437461G>CCA397125390ZNF469c.9991G>C (p.Ala3331Pro)
c.9907G>C (p.Ala3303Pro)
16g.88437461G>TCA397125391ZNF469c.9991G>T (p.Ala3331Ser)
c.9907G>T (p.Ala3303Ser)
gnomAD v4
16g.88437462C>ACA397125392ZNF469c.9992C>A (p.Ala3331Asp)
c.9908C>A (p.Ala3303Asp)
dbSNP gnomAD v2 gnomAD v4
16g.88437462C=CA2241073113ZNF469c.9992C= (p.Ala3331=)
c.9908C= (p.Ala3303=)
16g.88437462C>GCA397125393ZNF469c.9992C>G (p.Ala3331Gly)
c.9908C>G (p.Ala3303Gly)
16g.88437462C>TCA397125394ZNF469c.9992C>T (p.Ala3331Val)
c.9908C>T (p.Ala3303Val)
gnomAD v4
16g.88437463C>ACA497358591ZNF469c.9993C>A (p.Ala3331=)
c.9909C>A (p.Ala3303=)
gnomAD v4
16g.88437463C>GCA497358592ZNF469c.9993C>G (p.Ala3331=)
c.9909C>G (p.Ala3303=)
16g.88437463C>TCA497358593ZNF469c.9993C>T (p.Ala3331=)
c.9909C>T (p.Ala3303=)
16g.88437464T>ACA397125395ZNF469c.9994T>A (p.Cys3332Ser)
c.9910T>A (p.Cys3304Ser)
16g.88437464T>CCA397125396ZNF469c.9994T>C (p.Cys3332Arg)
c.9910T>C (p.Cys3304Arg)
gnomAD v4
16g.88437464T>GCA397125397ZNF469c.9994T>G (p.Cys3332Gly)
c.9910T>G (p.Cys3304Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437464T=CA2241073115ZNF469c.9994T= (p.Cys3332=)
c.9910T= (p.Cys3304=)
16g.88437465G>ACA397125398ZNF469c.9995G>A (p.Cys3332Tyr)
c.9911G>A (p.Cys3304Tyr)
gnomAD v4
16g.88437465G>CCA397125399ZNF469c.9995G>C (p.Cys3332Ser)
c.9911G>C (p.Cys3304Ser)
16g.88437465G>TCA397125400ZNF469c.9995G>T (p.Cys3332Phe)
c.9911G>T (p.Cys3304Phe)
gnomAD v4
16g.88437466C>ACA397125402ZNF469c.9996C>A (p.Cys3332Ter)
c.9912C>A (p.Cys3304Ter)
gnomAD v4
16g.88437466C>GCA397125401ZNF469c.9996C>G (p.Cys3332Trp)
c.9912C>G (p.Cys3304Trp)
16g.88437466C>TCA497358594ZNF469c.9996C>T (p.Cys3332=)
c.9912C>T (p.Cys3304=)
16g.88437467A>CCA397125403ZNF469c.9997A>C (p.Lys3333Gln)
c.9913A>C (p.Lys3305Gln)
16g.88437467A>GCA397125404ZNF469c.9997A>G (p.Lys3333Glu)
c.9913A>G (p.Lys3305Glu)
16g.88437467A>TCA397125405ZNF469c.9997A>T (p.Lys3333Ter)
c.9913A>T (p.Lys3305Ter)
16g.88437468A>CCA397125406ZNF469c.9998A>C (p.Lys3333Thr)
c.9914A>C (p.Lys3305Thr)
16g.88437468A>GCA397125407ZNF469c.9998A>G (p.Lys3333Arg)
c.9914A>G (p.Lys3305Arg)
16g.88437468A>TCA397125408ZNF469c.9998A>T (p.Lys3333Met)
c.9914A>T (p.Lys3305Met)
gnomAD v4
16g.88437469G>ACA8225467ZNF469c.9999G>A (p.Lys3333=)
c.9915G>A (p.Lys3305=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88437469G>CCA397125409ZNF469c.9999G>C (p.Lys3333Asn)
c.9915G>C (p.Lys3305Asn)
16g.88437469G=CA2241073118ZNF469c.9999G= (p.Lys3333=)
c.9915G= (p.Lys3305=)
16g.88437469G>TCA397125410ZNF469c.9999G>T (p.Lys3333Asn)
c.9915G>T (p.Lys3305Asn)
16g.88437470G>ACA397125411ZNF469c.10000G>A (p.Asp3334Asn)
c.9916G>A (p.Asp3306Asn)
gnomAD v4
16g.88437470G>CCA397125412ZNF469c.10000G>C (p.Asp3334His)
c.9916G>C (p.Asp3306His)
ClinVar dbSNP gnomAD v4
16g.88437470G=CA2241073120ZNF469c.10000G= (p.Asp3334=)
c.9916G= (p.Asp3306=)
16g.88437470G>TCA397125413ZNF469c.10000G>T (p.Asp3334Tyr)
c.9916G>T (p.Asp3306Tyr)
ClinVar
16g.88437471A>CCA397125416ZNF469c.10001A>C (p.Asp3334Ala)
c.9917A>C (p.Asp3306Ala)
16g.88437471A>GCA397125415ZNF469c.10001A>G (p.Asp3334Gly)
c.9917A>G (p.Asp3306Gly)
16g.88437471A>TCA397125414ZNF469c.10001A>T (p.Asp3334Val)
c.9917A>T (p.Asp3306Val)
16g.88437472C>ACA397125417ZNF469c.10002C>A (p.Asp3334Glu)
c.9918C>A (p.Asp3306Glu)
gnomAD v4
16g.88437472C>GCA397125418ZNF469c.10002C>G (p.Asp3334Glu)
c.9918C>G (p.Asp3306Glu)
16g.88437472C>TCA497358595ZNF469c.10002C>T (p.Asp3334=)
c.9918C>T (p.Asp3306=)
gnomAD v4
16g.88437473C>ACA397125419ZNF469c.10003C>A (p.Pro3335Thr)
c.9919C>A (p.Pro3307Thr)
dbSNP gnomAD v2 gnomAD v4
16g.88437473C=CA2241073122ZNF469c.10003C= (p.Pro3335=)
c.9919C= (p.Pro3307=)
16g.88437473C>GCA397125420ZNF469c.10003C>G (p.Pro3335Ala)
c.9919C>G (p.Pro3307Ala)
16g.88437473C>TCA397125421ZNF469c.10003C>T (p.Pro3335Ser)
c.9919C>T (p.Pro3307Ser)
ClinVar dbSNP gnomAD v4
16g.88437474C>ACA397125422ZNF469c.10004C>A (p.Pro3335His)
c.9920C>A (p.Pro3307His)
16g.88437474C=CA2241073123ZNF469c.10004C= (p.Pro3335=)
c.9920C= (p.Pro3307=)
16g.88437474C>GCA397125423ZNF469c.10004C>G (p.Pro3335Arg)
c.9920C>G (p.Pro3307Arg)
16g.88437474C>TCA397125424ZNF469c.10004C>T (p.Pro3335Leu)
c.9920C>T (p.Pro3307Leu)
dbSNP gnomAD v2 gnomAD v4
16g.88437475C>ACA497358596ZNF469c.10005C>A (p.Pro3335=)
c.9921C>A (p.Pro3307=)
16g.88437475C=CA2241073124ZNF469c.10005C= (p.Pro3335=)
c.9921C= (p.Pro3307=)
16g.88437475C>GCA497358597ZNF469c.10005C>G (p.Pro3335=)
c.9921C>G (p.Pro3307=)
16g.88437475C>TCA8225468ZNF469c.10005C>T (p.Pro3335=)
c.9921C>T (p.Pro3307=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88437476T>ACA397125425ZNF469c.10006T>A (p.Ser3336Thr)
c.9922T>A (p.Ser3308Thr)
16g.88437476T>CCA397125426ZNF469c.10006T>C (p.Ser3336Pro)
c.9922T>C (p.Ser3308Pro)
16g.88437476T>GCA397125427ZNF469c.10006T>G (p.Ser3336Ala)
c.9922T>G (p.Ser3308Ala)
16g.88437477C>ACA397125430ZNF469c.10007C>A (p.Ser3336Tyr)
c.9923C>A (p.Ser3308Tyr)
gnomAD v4
16g.88437477C=CA2241073126ZNF469c.10007C= (p.Ser3336=)
c.9923C= (p.Ser3308=)
16g.88437477C>GCA397125428ZNF469c.10007C>G (p.Ser3336Cys)
c.9923C>G (p.Ser3308Cys)
16g.88437477C>TCA397125429ZNF469c.10007C>T (p.Ser3336Phe)
c.9923C>T (p.Ser3308Phe)
dbSNP gnomAD v2
16g.88437478C>ACA497358599ZNF469c.10008C>A (p.Ser3336=)
c.9924C>A (p.Ser3308=)
gnomAD v4
16g.88437478C=CA2241073127ZNF469c.10008C= (p.Ser3336=)
c.9924C= (p.Ser3308=)
16g.88437478C>GCA497358600ZNF469c.10008C>G (p.Ser3336=)
c.9924C>G (p.Ser3308=)
16g.88437478C>TCA497358598ZNF469c.10008C>T (p.Ser3336=)
c.9924C>T (p.Ser3308=)
dbSNP gnomAD v3 gnomAD v4
16g.88437479C>ACA397125431ZNF469c.10009C>A (p.Arg3337Ser)
c.9925C>A (p.Arg3309Ser)
gnomAD v4 COSMIC
16g.88437479C>GCA397125432ZNF469c.10009C>G (p.Arg3337Gly)
c.9925C>G (p.Arg3309Gly)
16g.88437479C>TCA397125433ZNF469c.10009C>T (p.Arg3337Cys)
c.9925C>T (p.Arg3309Cys)
16g.88437480G>ACA8225469ZNF469c.10010G>A (p.Arg3337His)
c.9926G>A (p.Arg3309His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88437480G>CCA397125434ZNF469c.10010G>C (p.Arg3337Pro)
c.9926G>C (p.Arg3309Pro)
16g.88437480G=CA2241073129ZNF469c.10010G= (p.Arg3337=)
c.9926G= (p.Arg3309=)
16g.88437480G>TCA397125435ZNF469c.10010G>T (p.Arg3337Leu)
c.9926G>T (p.Arg3309Leu)
16g.88437481C>ACA497358601ZNF469c.10011C>A (p.Arg3337=)
c.9927C>A (p.Arg3309=)
dbSNP gnomAD v4
16g.88437481C=CA2241073131ZNF469c.10011C= (p.Arg3337=)
c.9927C= (p.Arg3309=)
16g.88437481C>GCA497358602ZNF469c.10011C>G (p.Arg3337=)
c.9927C>G (p.Arg3309=)
16g.88437481C>TCA286386067ZNF469c.10011C>T (p.Arg3337=)
c.9927C>T (p.Arg3309=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437482G>ACA8225470ZNF469c.10012G>A (p.Asp3338Asn)
c.9928G>A (p.Asp3310Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.88437482G>CCA397125436ZNF469c.10012G>C (p.Asp3338His)
c.9928G>C (p.Asp3310His)
16g.88437482G=CA2241073133ZNF469c.10012G= (p.Asp3338=)
c.9928G= (p.Asp3310=)
16g.88437482G>TCA397125437ZNF469c.10012G>T (p.Asp3338Tyr)
c.9928G>T (p.Asp3310Tyr)
ClinVar dbSNP gnomAD v4
16g.88437483A>CCA397125438ZNF469c.10013A>C (p.Asp3338Ala)
c.9929A>C (p.Asp3310Ala)
16g.88437483A>GCA397125439ZNF469c.10013A>G (p.Asp3338Gly)
c.9929A>G (p.Asp3310Gly)
16g.88437483A>TCA397125440ZNF469c.10013A>T (p.Asp3338Val)
c.9929A>T (p.Asp3310Val)
16g.88437484C>ACA397125441ZNF469c.10014C>A (p.Asp3338Glu)
c.9930C>A (p.Asp3310Glu)
gnomAD v4
16g.88437484C>GCA397125442ZNF469c.10014C>G (p.Asp3338Glu)
c.9930C>G (p.Asp3310Glu)
16g.88437484C>TCA497358603ZNF469c.10014C>T (p.Asp3338=)
c.9930C>T (p.Asp3310=)
ClinVar gnomAD v4
16g.88437485T>ACA397125443ZNF469c.10015T>A (p.Cys3339Ser)
c.9931T>A (p.Cys3311Ser)
16g.88437485T>CCA397125445ZNF469c.10015T>C (p.Cys3339Arg)
c.9931T>C (p.Cys3311Arg)
16g.88437485T>GCA397125444ZNF469c.10015T>G (p.Cys3339Gly)
c.9931T>G (p.Cys3311Gly)
16g.88437486G>ACA397125446ZNF469c.10016G>A (p.Cys3339Tyr)
c.9932G>A (p.Cys3311Tyr)
gnomAD v4
16g.88437486G>CCA397125447ZNF469c.10016G>C (p.Cys3339Ser)
c.9932G>C (p.Cys3311Ser)
16g.88437486G=CA2241073135ZNF469c.10016G= (p.Cys3339=)
c.9932G= (p.Cys3311=)
16g.88437486G>TCA286386071ZNF469c.10016G>T (p.Cys3339Phe)
c.9932G>T (p.Cys3311Phe)
dbSNP
16g.88437487C>ACA397125448ZNF469c.10017C>A (p.Cys3339Ter)
c.9933C>A (p.Cys3311Ter)
16g.88437487C>GCA397125449ZNF469c.10017C>G (p.Cys3339Trp)
c.9933C>G (p.Cys3311Trp)
16g.88437487C>TCA497358604ZNF469c.10017C>T (p.Cys3339=)
c.9933C>T (p.Cys3311=)
ClinVar gnomAD v4
16g.88437488C>ACA397125450ZNF469c.10018C>A (p.His3340Asn)
c.9934C>A (p.His3312Asn)
16g.88437488C>GCA397125451ZNF469c.10018C>G (p.His3340Asp)
c.9934C>G (p.His3312Asp)
16g.88437488C>TCA397125452ZNF469c.10018C>T (p.His3340Tyr)
c.9934C>T (p.His3312Tyr)
gnomAD v4
16g.88437489A>CCA397125453ZNF469c.10019A>C (p.His3340Pro)
c.9935A>C (p.His3312Pro)
16g.88437489A>GCA397125454ZNF469c.10019A>G (p.His3340Arg)
c.9935A>G (p.His3312Arg)
16g.88437489A>TCA397125455ZNF469c.10019A>T (p.His3340Leu)
c.9935A>T (p.His3312Leu)
COSMIC
16g.88437490C>ACA397125456ZNF469c.10020C>A (p.His3340Gln)
c.9936C>A (p.His3312Gln)
16g.88437490C=CA2241073137ZNF469c.10020C= (p.His3340=)
c.9936C= (p.His3312=)
16g.88437490C>GCA397125457ZNF469c.10020C>G (p.His3340Gln)
c.9936C>G (p.His3312Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437490C>TCA497358605ZNF469c.10020C>T (p.His3340=)
c.9936C>T (p.His3312=)
gnomAD v4
16g.88437491C>ACA397125458ZNF469c.10021C>A (p.His3341Asn)
c.9937C>A (p.His3313Asn)
16g.88437491C>GCA397125460ZNF469c.10021C>G (p.His3341Asp)
c.9937C>G (p.His3313Asp)
16g.88437491C>TCA397125459ZNF469c.10021C>T (p.His3341Tyr)
c.9937C>T (p.His3313Tyr)
16g.88437492A>CCA397125461ZNF469c.10022A>C (p.His3341Pro)
c.9938A>C (p.His3313Pro)
16g.88437492A>GCA397125462ZNF469c.10022A>G (p.His3341Arg)
c.9938A>G (p.His3313Arg)
16g.88437492A>TCA397125463ZNF469c.10022A>T (p.His3341Leu)
c.9938A>T (p.His3313Leu)
16g.88437493C>ACA397125464ZNF469c.10023C>A (p.His3341Gln)
c.9939C>A (p.His3313Gln)
16g.88437493C>GCA397125465ZNF469c.10023C>G (p.His3341Gln)
c.9939C>G (p.His3313Gln)
16g.88437493C>TCA497358606ZNF469c.10023C>T (p.His3341=)
c.9939C>T (p.His3313=)
16g.88437494T>ACA397125466ZNF469c.10024T>A (p.Cys3342Ser)
c.9940T>A (p.Cys3314Ser)
16g.88437494T>CCA397125467ZNF469c.10024T>C (p.Cys3342Arg)
c.9940T>C (p.Cys3314Arg)
16g.88437494T>GCA397125468ZNF469c.10024T>G (p.Cys3342Gly)
c.9940T>G (p.Cys3314Gly)
gnomAD v4
16g.88437495G>ACA397125469ZNF469c.10025G>A (p.Cys3342Tyr)
c.9941G>A (p.Cys3314Tyr)
16g.88437495G>CCA397125470ZNF469c.10025G>C (p.Cys3342Ser)
c.9941G>C (p.Cys3314Ser)
16g.88437495G>TCA397125471ZNF469c.10025G>T (p.Cys3342Phe)
c.9941G>T (p.Cys3314Phe)
16g.88437496C>ACA397125472ZNF469c.10026C>A (p.Cys3342Ter)
c.9942C>A (p.Cys3314Ter)
16g.88437496C>GCA397125473ZNF469c.10026C>G (p.Cys3342Trp)
c.9942C>G (p.Cys3314Trp)
16g.88437496C>TCA497358607ZNF469c.10026C>T (p.Cys3342=)
c.9942C>T (p.Cys3314=)
gnomAD v4
16g.88437497G>ACA397125474ZNF469c.10027G>A (p.Gly3343Arg)
c.9943G>A (p.Gly3315Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437497G>CCA397125475ZNF469c.10027G>C (p.Gly3343Arg)
c.9943G>C (p.Gly3315Arg)
COSMIC
16g.88437497G=CA2241073139ZNF469c.10027G= (p.Gly3343=)
c.9943G= (p.Gly3315=)
16g.88437497G>TCA397125476ZNF469c.10027G>T (p.Gly3343Trp)
c.9943G>T (p.Gly3315Trp)
gnomAD v4
16g.88437498G>ACA397125477ZNF469c.10028G>A (p.Gly3343Glu)
c.9944G>A (p.Gly3315Glu)
dbSNP gnomAD v4 COSMIC
16g.88437498G>CCA397125478ZNF469c.10028G>C (p.Gly3343Ala)
c.9944G>C (p.Gly3315Ala)
16g.88437498G=CA2241073141ZNF469c.10028G= (p.Gly3343=)
c.9944G= (p.Gly3315=)
16g.88437498G>TCA397125479ZNF469c.10028G>T (p.Gly3343Val)
c.9944G>T (p.Gly3315Val)
16g.88437499G>ACA497358608ZNF469c.10029G>A (p.Gly3343=)
c.9945G>A (p.Gly3315=)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88437499G>CCA497358610ZNF469c.10029G>C (p.Gly3343=)
c.9945G>C (p.Gly3315=)
16g.88437499G=CA2241073143ZNF469c.10029G= (p.Gly3343=)
c.9945G= (p.Gly3315=)
16g.88437499G>TCA497358609ZNF469c.10029G>T (p.Gly3343=)
c.9945G>T (p.Gly3315=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88437500A>CCA397125482ZNF469c.10030A>C (p.Lys3344Gln)
c.9946A>C (p.Lys3316Gln)
16g.88437500A>GCA397125480ZNF469c.10030A>G (p.Lys3344Glu)
c.9946A>G (p.Lys3316Glu)
16g.88437500A>TCA397125481ZNF469c.10030A>T (p.Lys3344Ter)
c.9946A>T (p.Lys3316Ter)
16g.88437501A>CCA397125483ZNF469c.10031A>C (p.Lys3344Thr)
c.9947A>C (p.Lys3316Thr)
16g.88437501A>GCA397125484ZNF469c.10031A>G (p.Lys3344Arg)
c.9947A>G (p.Lys3316Arg)
gnomAD v4
16g.88437501A>TCA397125485ZNF469c.10031A>T (p.Lys3344Met)
c.9947A>T (p.Lys3316Met)
16g.88437502G>ACA497358666ZNF469c.10032G>A (p.Lys3344=)
c.9948G>A (p.Lys3316=)
gnomAD v4
16g.88437502G>CCA397125486ZNF469c.10032G>C (p.Lys3344Asn)
c.9948G>C (p.Lys3316Asn)
16g.88437502G>TCA397125487ZNF469c.10032G>T (p.Lys3344Asn)
c.9948G>T (p.Lys3316Asn)
gnomAD v4
16g.88437502dupCA2634824482ZNF469c.10032dup (p.Arg3345AlafsTer?)
c.9948dup (p.Arg3317AlafsTer?)
gnomAD v4
16g.88437503C>ACA397125488ZNF469c.10033C>A (p.Arg3345Ser)
c.9949C>A (p.Arg3317Ser)
16g.88437503C=CA2241073144ZNF469c.10033C= (p.Arg3345=)
c.9949C= (p.Arg3317=)
16g.88437503C>GCA397125490ZNF469c.10033C>G (p.Arg3345Gly)
c.9949C>G (p.Arg3317Gly)
dbSNP gnomAD v4
16g.88437503C>TCA397125489ZNF469c.10033C>T (p.Arg3345Cys)
c.9949C>T (p.Arg3317Cys)
gnomAD v4
16g.88437504G>ACA8225471ZNF469c.10034G>A (p.Arg3345His)
c.9950G>A (p.Arg3317His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88437504G>CCA397125491ZNF469c.10034G>C (p.Arg3345Pro)
c.9950G>C (p.Arg3317Pro)
16g.88437504G=CA2241073145ZNF469c.10034G= (p.Arg3345=)
c.9950G= (p.Arg3317=)
16g.88437504G>TCA397125492ZNF469c.10034G>T (p.Arg3345Leu)
c.9950G>T (p.Arg3317Leu)
16g.88437505C>ACA497358669ZNF469c.10035C>A (p.Arg3345=)
c.9951C>A (p.Arg3317=)
16g.88437505C=CA2241073148ZNF469c.10035C= (p.Arg3345=)
c.9951C= (p.Arg3317=)
16g.88437505C>GCA497358670ZNF469c.10035C>G (p.Arg3345=)
c.9951C>G (p.Arg3317=)
16g.88437505C>TCA497358671ZNF469c.10035C>T (p.Arg3345=)
c.9951C>T (p.Arg3317=)
dbSNP
16g.88437506T>ACA397125493ZNF469c.10036T>A (p.Phe3346Ile)
c.9952T>A (p.Phe3318Ile)
16g.88437506T>CCA397125494ZNF469c.10036T>C (p.Phe3346Leu)
c.9952T>C (p.Phe3318Leu)
gnomAD v4
16g.88437506T>GCA397125495ZNF469c.10036T>G (p.Phe3346Val)
c.9952T>G (p.Phe3318Val)
16g.88437507T>ACA397125496ZNF469c.10037T>A (p.Phe3346Tyr)
c.9953T>A (p.Phe3318Tyr)
16g.88437507T>CCA397125497ZNF469c.10037T>C (p.Phe3346Ser)
c.9953T>C (p.Phe3318Ser)
16g.88437507T>GCA397125498ZNF469c.10037T>G (p.Phe3346Cys)
c.9953T>G (p.Phe3318Cys)
16g.88437508C>ACA397125499ZNF469c.10038C>A (p.Phe3346Leu)
c.9954C>A (p.Phe3318Leu)
16g.88437508C=CA2241073149ZNF469c.10038C= (p.Phe3346=)
c.9954C= (p.Phe3318=)
16g.88437508C>GCA397125500ZNF469c.10038C>G (p.Phe3346Leu)
c.9954C>G (p.Phe3318Leu)
16g.88437508C>TCA286386093ZNF469c.10038C>T (p.Phe3346=)
c.9954C>T (p.Phe3318=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88437511dupCA2510481487ZNF469c.10041dup (p.Lys3348GlnfsTer?)
c.9957dup (p.Lys3320GlnfsTer?)
16g.88437509C>ACA397125501ZNF469c.10039C>A (p.Pro3347Thr)
c.9955C>A (p.Pro3319Thr)
16g.88437509C=CA2241073151ZNF469c.10039C= (p.Pro3347=)
c.9955C= (p.Pro3319=)
16g.88437509C>GCA397125502ZNF469c.10039C>G (p.Pro3347Ala)
c.9955C>G (p.Pro3319Ala)
16g.88437509C>TCA286386103ZNF469c.10039C>T (p.Pro3347Ser)
c.9955C>T (p.Pro3319Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88437510C>ACA397125504ZNF469c.10040C>A (p.Pro3347His)
c.9956C>A (p.Pro3319His)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88437510C=CA2241073152ZNF469c.10040C= (p.Pro3347=)
c.9956C= (p.Pro3319=)
16g.88437510C>GCA397125503ZNF469c.10040C>G (p.Pro3347Arg)
c.9956C>G (p.Pro3319Arg)
gnomAD v4
16g.88437510C>TCA397125505ZNF469c.10040C>T (p.Pro3347Leu)
c.9956C>T (p.Pro3319Leu)
ClinVar
16g.88437511C>ACA497358676ZNF469c.10041C>A (p.Pro3347=)
c.9957C>A (p.Pro3319=)
dbSNP gnomAD v2 gnomAD v4
16g.88437511C=CA2241073154ZNF469c.10041C= (p.Pro3347=)
c.9957C= (p.Pro3319=)
16g.88437511C>GCA497358677ZNF469c.10041C>G (p.Pro3347=)
c.9957C>G (p.Pro3319=)
16g.88437511C>TCA497358678ZNF469c.10041C>T (p.Pro3347=)
c.9957C>T (p.Pro3319=)
16g.88437512A>CCA397125506ZNF469c.10042A>C (p.Lys3348Gln)
c.9958A>C (p.Lys3320Gln)
16g.88437512A>GCA397125508ZNF469c.10042A>G (p.Lys3348Glu)
c.9958A>G (p.Lys3320Glu)
gnomAD v4
16g.88437512A>TCA397125507ZNF469c.10042A>T (p.Lys3348Ter)
c.9958A>T (p.Lys3320Ter)
16g.88437513A=CA2241073155ZNF469c.10043A= (p.Lys3348=)
c.9959A= (p.Lys3320=)
16g.88437513A>CCA397125509ZNF469c.10043A>C (p.Lys3348Thr)
c.9959A>C (p.Lys3320Thr)
16g.88437513A>GCA397125511ZNF469c.10043A>G (p.Lys3348Arg)
c.9959A>G (p.Lys3320Arg)
dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.88437513A>TCA397125510ZNF469c.10043A>T (p.Lys3348Met)
c.9959A>T (p.Lys3320Met)
16g.88437514G>ACA497358683ZNF469c.10044G>A (p.Lys3348=)
c.9960G>A (p.Lys3320=)
16g.88437514G>CCA397125512ZNF469c.10044G>C (p.Lys3348Asn)
c.9960G>C (p.Lys3320Asn)
gnomAD v4
16g.88437514G>TCA397125513ZNF469c.10044G>T (p.Lys3348Asn)
c.9960G>T (p.Lys3320Asn)
16g.88437515C>ACA397125514ZNF469c.10045C>A (p.Pro3349Thr)
c.9961C>A (p.Pro3321Thr)
gnomAD v4
16g.88437515C>GCA397125515ZNF469c.10045C>G (p.Pro3349Ala)
c.9961C>G (p.Pro3321Ala)
16g.88437515C>TCA397125516ZNF469c.10045C>T (p.Pro3349Ser)
c.9961C>T (p.Pro3321Ser)
16g.88437516C>ACA397125517ZNF469c.10046C>A (p.Pro3349His)
c.9962C>A (p.Pro3321His)
16g.88437516C>GCA397125518ZNF469c.10046C>G (p.Pro3349Arg)
c.9962C>G (p.Pro3321Arg)
16g.88437516C>TCA397125519ZNF469c.10046C>T (p.Pro3349Leu)
c.9962C>T (p.Pro3321Leu)
16g.88437517C>ACA497358688ZNF469c.10047C>A (p.Pro3349=)
c.9963C>A (p.Pro3321=)
16g.88437517C=CA2241073156ZNF469c.10047C= (p.Pro3349=)
c.9963C= (p.Pro3321=)
16g.88437517C>GCA497358689ZNF469c.10047C>G (p.Pro3349=)
c.9963C>G (p.Pro3321=)
16g.88437517C>TCA286386104ZNF469c.10047C>T (p.Pro3349=)
c.9963C>T (p.Pro3321=)
ClinVar dbSNP gnomAD v4
16g.88437518T>ACA397125520ZNF469c.10048T>A (p.Phe3350Ile)
c.9964T>A (p.Phe3322Ile)
16g.88437518T>CCA397125521ZNF469c.10048T>C (p.Phe3350Leu)
c.9964T>C (p.Phe3322Leu)
16g.88437518T>GCA397125522ZNF469c.10048T>G (p.Phe3350Val)
c.9964T>G (p.Phe3322Val)
16g.88437519T>ACA397125525ZNF469c.10049T>A (p.Phe3350Tyr)
c.9965T>A (p.Phe3322Tyr)
16g.88437519T>CCA397125524ZNF469c.10049T>C (p.Phe3350Ser)
c.9965T>C (p.Phe3322Ser)
gnomAD v4
16g.88437519T>GCA397125523ZNF469c.10049T>G (p.Phe3350Cys)
c.9965T>G (p.Phe3322Cys)
16g.88437520C>ACA397125526ZNF469c.10050C>A (p.Phe3350Leu)
c.9966C>A (p.Phe3322Leu)
16g.88437520C=CA2241073158ZNF469c.10050C= (p.Phe3350=)
c.9966C= (p.Phe3322=)
16g.88437520C>GCA397125527ZNF469c.10050C>G (p.Phe3350Leu)
c.9966C>G (p.Phe3322Leu)
dbSNP gnomAD v2
16g.88437520C>TCA497358691ZNF469c.10050C>T (p.Phe3350=)
c.9966C>T (p.Phe3322=)
gnomAD v4
16g.88437521A>CCA397125528ZNF469c.10051A>C (p.Lys3351Gln)
c.9967A>C (p.Lys3323Gln)
gnomAD v4
16g.88437521A>GCA397125529ZNF469c.10051A>G (p.Lys3351Glu)
c.9967A>G (p.Lys3323Glu)
16g.88437521A>TCA397125530ZNF469c.10051A>T (p.Lys3351Ter)
c.9967A>T (p.Lys3323Ter)
16g.88437522A=CA2241073159ZNF469c.10052A= (p.Lys3351=)
c.9968A= (p.Lys3323=)
16g.88437522A>CCA397125531ZNF469c.10052A>C (p.Lys3351Thr)
c.9968A>C (p.Lys3323Thr)
16g.88437522A>GCA397125532ZNF469c.10052A>G (p.Lys3351Arg)
c.9968A>G (p.Lys3323Arg)
dbSNP gnomAD v3 gnomAD v4
16g.88437522A>TCA397125533ZNF469c.10052A>T (p.Lys3351Met)
c.9968A>T (p.Lys3323Met)
gnomAD v4
16g.88437523G>ACA497358695ZNF469c.10053G>A (p.Lys3351=)
c.9969G>A (p.Lys3323=)
gnomAD v4
16g.88437523G>CCA397125534ZNF469c.10053G>C (p.Lys3351Asn)
c.9969G>C (p.Lys3323Asn)
16g.88437523G>TCA397125535ZNF469c.10053G>T (p.Lys3351Asn)
c.9969G>T (p.Lys3323Asn)
gnomAD v4
16g.88437524C>ACA397125536ZNF469c.10054C>A (p.Leu3352Met)
c.9970C>A (p.Leu3324Met)
16g.88437524C>GCA397125537ZNF469c.10054C>G (p.Leu3352Val)
c.9970C>G (p.Leu3324Val)
16g.88437524C>TCA497358697ZNF469c.10054C>T (p.Leu3352=)
c.9970C>T (p.Leu3324=)
16g.88437525T>ACA397125539ZNF469c.10055T>A (p.Leu3352Gln)
c.9971T>A (p.Leu3324Gln)
16g.88437525T>CCA397125540ZNF469c.10055T>C (p.Leu3352Pro)
c.9971T>C (p.Leu3324Pro)
gnomAD v4
16g.88437525T>GCA397125538ZNF469c.10055T>G (p.Leu3352Arg)
c.9971T>G (p.Leu3324Arg)
16g.88437526G>ACA497358698ZNF469c.10056G>A (p.Leu3352=)
c.9972G>A (p.Leu3324=)
gnomAD v4
16g.88437526G>CCA497358701ZNF469c.10056G>C (p.Leu3352=)
c.9972G>C (p.Leu3324=)
16g.88437526G>TCA497358700ZNF469c.10056G>T (p.Leu3352=)
c.9972G>T (p.Leu3324=)
16g.88437527C>ACA397125541ZNF469c.10057C>A (p.Gln3353Lys)
c.9973C>A (p.Gln3325Lys)
16g.88437527C>GCA397125542ZNF469c.10057C>G (p.Gln3353Glu)
c.9973C>G (p.Gln3325Glu)
16g.88437527C>TCA397125543ZNF469c.10057C>T (p.Gln3353Ter)
c.9973C>T (p.Gln3325Ter)
gnomAD v4
16g.88437528A>CCA397125544ZNF469c.10058A>C (p.Gln3353Pro)
c.9974A>C (p.Gln3325Pro)
16g.88437528A>GCA397125546ZNF469c.10058A>G (p.Gln3353Arg)
c.9974A>G (p.Gln3325Arg)
gnomAD v4
16g.88437528A>TCA397125547ZNF469c.10058A>T (p.Gln3353Leu)
c.9974A>T (p.Gln3325Leu)
16g.88437529G>ACA497358702ZNF469c.10059G>A (p.Gln3353=)
c.9975G>A (p.Gln3325=)
16g.88437529G>CCA397125550ZNF469c.10059G>C (p.Gln3353His)
c.9975G>C (p.Gln3325His)
16g.88437529G>TCA397125551ZNF469c.10059G>T (p.Gln3353His)
c.9975G>T (p.Gln3325His)
gnomAD v4
16g.88437530C>ACA397125552ZNF469c.10060C>A (p.Arg3354Ser)
c.9976C>A (p.Arg3326Ser)
gnomAD v4
16g.88437530C=CA2241073161ZNF469c.10060C= (p.Arg3354=)
c.9976C= (p.Arg3326=)
16g.88437530C>GCA397125554ZNF469c.10060C>G (p.Arg3354Gly)
c.9976C>G (p.Arg3326Gly)
16g.88437530C>TCA397125556ZNF469c.10060C>T (p.Arg3354Cys)
c.9976C>T (p.Arg3326Cys)
dbSNP gnomAD v2 gnomAD v4
16g.88437531G>ACA397125558ZNF469c.10061G>A (p.Arg3354His)
c.9977G>A (p.Arg3326His)
gnomAD v4
16g.88437531G>CCA397125560ZNF469c.10061G>C (p.Arg3354Pro)
c.9977G>C (p.Arg3326Pro)
16g.88437531G>TCA397125557ZNF469c.10061G>T (p.Arg3354Leu)
c.9977G>T (p.Arg3326Leu)
gnomAD v4
16g.88437532C>ACA497358706ZNF469c.10062C>A (p.Arg3354=)
c.9978C>A (p.Arg3326=)
gnomAD v4
16g.88437532C=CA2241073163ZNF469c.10062C= (p.Arg3354=)
c.9978C= (p.Arg3326=)
16g.88437532C>GCA497358707ZNF469c.10062C>G (p.Arg3354=)
c.9978C>G (p.Arg3326=)
16g.88437532C>TCA497358708ZNF469c.10062C>T (p.Arg3354=)
c.9978C>T (p.Arg3326=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88437533C>ACA397125562ZNF469c.10063C>A (p.His3355Asn)
c.9979C>A (p.His3327Asn)
16g.88437533C>GCA397125563ZNF469c.10063C>G (p.His3355Asp)
c.9979C>G (p.His3327Asp)
16g.88437533C>TCA397125565ZNF469c.10063C>T (p.His3355Tyr)
c.9979C>T (p.His3327Tyr)
COSMIC
16g.88437534A>CCA397125566ZNF469c.10064A>C (p.His3355Pro)
c.9980A>C (p.His3327Pro)
16g.88437534A>GCA397125567ZNF469c.10064A>G (p.His3355Arg)
c.9980A>G (p.His3327Arg)
16g.88437534A>TCA397125568ZNF469c.10064A>T (p.His3355Leu)
c.9980A>T (p.His3327Leu)
16g.88437535C>ACA397125570ZNF469c.10065C>A (p.His3355Gln)
c.9981C>A (p.His3327Gln)
16g.88437535C>GCA397125572ZNF469c.10065C>G (p.His3355Gln)
c.9981C>G (p.His3327Gln)
16g.88437535C>TCA497358710ZNF469c.10065C>T (p.His3355=)
c.9981C>T (p.His3327=)
16g.88437536C>ACA397125573ZNF469c.10066C>A (p.Leu3356Met)
c.9982C>A (p.Leu3328Met)
gnomAD v4
16g.88437536C>GCA397125575ZNF469c.10066C>G (p.Leu3356Val)
c.9982C>G (p.Leu3328Val)
16g.88437536C>TCA497358713ZNF469c.10066C>T (p.Leu3356=)
c.9982C>T (p.Leu3328=)
16g.88437537T>ACA397125576ZNF469c.10067T>A (p.Leu3356Gln)
c.9983T>A (p.Leu3328Gln)
16g.88437537T>CCA397125578ZNF469c.10067T>C (p.Leu3356Pro)
c.9983T>C (p.Leu3328Pro)
gnomAD v4
16g.88437537T>GCA16620287ZNF469c.10067T>G (p.Leu3356Arg)
c.9983T>G (p.Leu3328Arg)
ClinVar dbSNP
16g.88437537T=CA2241073165ZNF469c.10067T= (p.Leu3356=)
c.9983T= (p.Leu3328=)
16g.88437538G>ACA497358715ZNF469c.10068G>A (p.Leu3356=)
c.9984G>A (p.Leu3328=)
gnomAD v4
16g.88437538G>CCA497358716ZNF469c.10068G>C (p.Leu3356=)
c.9984G>C (p.Leu3328=)
16g.88437538G>TCA497358717ZNF469c.10068G>T (p.Leu3356=)
c.9984G>T (p.Leu3328=)
gnomAD v4
16g.88437539G>ACA397125583ZNF469c.10069G>A (p.Ala3357Thr)
c.9985G>A (p.Ala3329Thr)
16g.88437539G>CCA397125582ZNF469c.10069G>C (p.Ala3357Pro)
c.9985G>C (p.Ala3329Pro)
16g.88437539G>TCA397125580ZNF469c.10069G>T (p.Ala3357Ser)
c.9985G>T (p.Ala3329Ser)
gnomAD v4
16g.88437540C>ACA397125584ZNF469c.10070C>A (p.Ala3357Glu)
c.9986C>A (p.Ala3329Glu)
16g.88437540C=CA2241073168ZNF469c.10070C= (p.Ala3357=)
c.9986C= (p.Ala3329=)
16g.88437540C>GCA397125588ZNF469c.10070C>G (p.Ala3357Gly)
c.9986C>G (p.Ala3329Gly)
16g.88437540C>TCA397125586ZNF469c.10070C>T (p.Ala3357Val)
c.9986C>T (p.Ala3329Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched