Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.88439047_88439080dupCA2634824416ZNF469c.11577_11610dup (p.Arg3871AspfsTer?)
c.11493_11526dup (p.Arg3843AspfsTer?)
gnomAD v4
16g.88439069C>ACA397130658ZNF469c.11599C>A (p.Gln3867Lys)
c.11515C>A (p.Gln3839Lys)
16g.88439069C=CA2241074217ZNF469c.11599C= (p.Gln3867=)
c.11515C= (p.Gln3839=)
16g.88439069C>GCA397130659ZNF469c.11599C>G (p.Gln3867Glu)
c.11515C>G (p.Gln3839Glu)
dbSNP
16g.88439069C>TCA286388283ZNF469c.11599C>T (p.Gln3867Ter)
c.11515C>T (p.Gln3839Ter)
dbSNP gnomAD v4
16g.88439070A=CA2241074221ZNF469c.11600A= (p.Gln3867=)
c.11516A= (p.Gln3839=)
16g.88439070A>CCA397130660ZNF469c.11600A>C (p.Gln3867Pro)
c.11516A>C (p.Gln3839Pro)
16g.88439070A>GCA397130661ZNF469c.11600A>G (p.Gln3867Arg)
c.11516A>G (p.Gln3839Arg)
gnomAD v4
16g.88439070A>TCA397130662ZNF469c.11600A>T (p.Gln3867Leu)
c.11516A>T (p.Gln3839Leu)
dbSNP gnomAD v2 gnomAD v4
16g.88439071G>ACA497359519ZNF469c.11601G>A (p.Gln3867=)
c.11517G>A (p.Gln3839=)
ClinVar gnomAD v4
16g.88439071G>CCA397130663ZNF469c.11601G>C (p.Gln3867His)
c.11517G>C (p.Gln3839His)
16g.88439071G>TCA397130664ZNF469c.11601G>T (p.Gln3867His)
c.11517G>T (p.Gln3839His)
16g.88439072A>CCA397130665ZNF469c.11602A>C (p.Asn3868His)
c.11518A>C (p.Asn3840His)
16g.88439072A>GCA397130666ZNF469c.11602A>G (p.Asn3868Asp)
c.11518A>G (p.Asn3840Asp)
16g.88439072A>TCA397130667ZNF469c.11602A>T (p.Asn3868Tyr)
c.11518A>T (p.Asn3840Tyr)
16g.88439073A=CA2241074224ZNF469c.11603A= (p.Asn3868=)
c.11519A= (p.Asn3840=)
16g.88439073A>CCA397130670ZNF469c.11603A>C (p.Asn3868Thr)
c.11519A>C (p.Asn3840Thr)
16g.88439073A>GCA397130668ZNF469c.11603A>G (p.Asn3868Ser)
c.11519A>G (p.Asn3840Ser)
dbSNP
16g.88439073A>TCA397130669ZNF469c.11603A>T (p.Asn3868Ile)
c.11519A>T (p.Asn3840Ile)
16g.88439074C>ACA397130671ZNF469c.11604C>A (p.Asn3868Lys)
c.11520C>A (p.Asn3840Lys)
dbSNP gnomAD v2 gnomAD v4
16g.88439074C=CA2241074227ZNF469c.11604C= (p.Asn3868=)
c.11520C= (p.Asn3840=)
16g.88439074C>GCA397130672ZNF469c.11604C>G (p.Asn3868Lys)
c.11520C>G (p.Asn3840Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439074C>TCA497359520ZNF469c.11604C>T (p.Asn3868=)
c.11520C>T (p.Asn3840=)
16g.88439075A>CCA397130673ZNF469c.11605A>C (p.Lys3869Gln)
c.11521A>C (p.Lys3841Gln)
16g.88439075A>GCA397130674ZNF469c.11605A>G (p.Lys3869Glu)
c.11521A>G (p.Lys3841Glu)
16g.88439075A>TCA397130675ZNF469c.11605A>T (p.Lys3869Ter)
c.11521A>T (p.Lys3841Ter)
16g.88439076A>CCA397130676ZNF469c.11606A>C (p.Lys3869Thr)
c.11522A>C (p.Lys3841Thr)
16g.88439076A>GCA397130677ZNF469c.11606A>G (p.Lys3869Arg)
c.11522A>G (p.Lys3841Arg)
16g.88439076A>TCA397130678ZNF469c.11606A>T (p.Lys3869Ile)
c.11522A>T (p.Lys3841Ile)
16g.88439077A>CCA397130679ZNF469c.11607A>C (p.Lys3869Asn)
c.11523A>C (p.Lys3841Asn)
16g.88439077A>GCA497359521ZNF469c.11607A>G (p.Lys3869=)
c.11523A>G (p.Lys3841=)
16g.88439077A>TCA397130680ZNF469c.11607A>T (p.Lys3869Asn)
c.11523A>T (p.Lys3841Asn)
16g.88439078C>ACA397130681ZNF469c.11608C>A (p.Pro3870Thr)
c.11524C>A (p.Pro3842Thr)
dbSNP gnomAD v2 gnomAD v4
16g.88439078C=CA2241074229ZNF469c.11608C= (p.Pro3870=)
c.11524C= (p.Pro3842=)
16g.88439078C>GCA397130682ZNF469c.11608C>G (p.Pro3870Ala)
c.11524C>G (p.Pro3842Ala)
gnomAD v4
16g.88439078C>TCA397130683ZNF469c.11608C>T (p.Pro3870Ser)
c.11524C>T (p.Pro3842Ser)
16g.88439079C>ACA397130684ZNF469c.11609C>A (p.Pro3870His)
c.11525C>A (p.Pro3842His)
16g.88439079C=CA2241074231ZNF469c.11609C= (p.Pro3870=)
c.11525C= (p.Pro3842=)
16g.88439079C>GCA397130685ZNF469c.11609C>G (p.Pro3870Arg)
c.11525C>G (p.Pro3842Arg)
gnomAD v4
16g.88439079C>TCA8225628ZNF469c.11609C>T (p.Pro3870Leu)
c.11525C>T (p.Pro3842Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439080C>ACA497359522ZNF469c.11610C>A (p.Pro3870=)
c.11526C>A (p.Pro3842=)
16g.88439080C>GCA497359523ZNF469c.11610C>G (p.Pro3870=)
c.11526C>G (p.Pro3842=)
16g.88439080C>TCA497359524ZNF469c.11610C>T (p.Pro3870=)
c.11526C>T (p.Pro3842=)
16g.88439081A=CA2241074234ZNF469c.11611A= (p.Arg3871=)
c.11527A= (p.Arg3843=)
16g.88439081A>CCA497359525ZNF469c.11611A>C (p.Arg3871=)
c.11527A>C (p.Arg3843=)
16g.88439081A>GCA397130686ZNF469c.11611A>G (p.Arg3871Gly)
c.11527A>G (p.Arg3843Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439081A>TCA397130687ZNF469c.11611A>T (p.Arg3871Trp)
c.11527A>T (p.Arg3843Trp)
16g.88439082G>ACA397130688ZNF469c.11612G>A (p.Arg3871Lys)
c.11528G>A (p.Arg3843Lys)
16g.88439082G>CCA397130690ZNF469c.11612G>C (p.Arg3871Thr)
c.11528G>C (p.Arg3843Thr)
16g.88439082G>TCA397130689ZNF469c.11612G>T (p.Arg3871Met)
c.11528G>T (p.Arg3843Met)
16g.88439083G>ACA497359526ZNF469c.11613G>A (p.Arg3871=)
c.11529G>A (p.Arg3843=)
16g.88439083G>CCA397130691ZNF469c.11613G>C (p.Arg3871Ser)
c.11529G>C (p.Arg3843Ser)
dbSNP
16g.88439083G>TCA397130692ZNF469c.11613G>T (p.Arg3871Ser)
c.11529G>T (p.Arg3843Ser)
16g.88439084C>ACA8225629ZNF469c.11614C>A (p.Pro3872Thr)
c.11530C>A (p.Pro3844Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439084C=CA2241074235ZNF469c.11614C= (p.Pro3872=)
c.11530C= (p.Pro3844=)
16g.88439084C>GCA397130694ZNF469c.11614C>G (p.Pro3872Ala)
c.11530C>G (p.Pro3844Ala)
16g.88439084C>TCA397130693ZNF469c.11614C>T (p.Pro3872Ser)
c.11530C>T (p.Pro3844Ser)
dbSNP gnomAD v2 gnomAD v4
16g.88439085C>ACA397130696ZNF469c.11615C>A (p.Pro3872Gln)
c.11531C>A (p.Pro3844Gln)
gnomAD v4
16g.88439085C=CA2241074239ZNF469c.11615C= (p.Pro3872=)
c.11531C= (p.Pro3844=)
16g.88439085C>GCA397130698ZNF469c.11615C>G (p.Pro3872Arg)
c.11531C>G (p.Pro3844Arg)
16g.88439085C>TCA286388312ZNF469c.11615C>T (p.Pro3872Leu)
c.11531C>T (p.Pro3844Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439086G>ACA286388320ZNF469c.11616G>A (p.Pro3872=)
c.11532G>A (p.Pro3844=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439086G>CCA497359527ZNF469c.11616G>C (p.Pro3872=)
c.11532G>C (p.Pro3844=)
16g.88439086G=CA2241074241ZNF469c.11616G= (p.Pro3872=)
c.11532G= (p.Pro3844=)
16g.88439086G>TCA497359528ZNF469c.11616G>T (p.Pro3872=)
c.11532G>T (p.Pro3844=)
16g.88439087C>ACA397130700ZNF469c.11617C>A (p.Pro3873Thr)
c.11533C>A (p.Pro3845Thr)
16g.88439087C=CA2241074244ZNF469c.11617C= (p.Pro3873=)
c.11533C= (p.Pro3845=)
16g.88439087C>GCA397130702ZNF469c.11617C>G (p.Pro3873Ala)
c.11533C>G (p.Pro3845Ala)
16g.88439087C>TCA397130704ZNF469c.11617C>T (p.Pro3873Ser)
c.11533C>T (p.Pro3845Ser)
dbSNP gnomAD v2 gnomAD v4
16g.88439088C>ACA397130706ZNF469c.11618C>A (p.Pro3873Gln)
c.11534C>A (p.Pro3845Gln)
16g.88439088C>GCA397130707ZNF469c.11618C>G (p.Pro3873Arg)
c.11534C>G (p.Pro3845Arg)
16g.88439088C>TCA397130708ZNF469c.11618C>T (p.Pro3873Leu)
c.11534C>T (p.Pro3845Leu)
gnomAD v4
16g.88439089A>CCA497359529ZNF469c.11619A>C (p.Pro3873=)
c.11535A>C (p.Pro3845=)
16g.88439089A>GCA497359531ZNF469c.11619A>G (p.Pro3873=)
c.11535A>G (p.Pro3845=)
16g.88439089A>TCA497359530ZNF469c.11619A>T (p.Pro3873=)
c.11535A>T (p.Pro3845=)
16g.88439090C>ACA397130710ZNF469c.11620C>A (p.Pro3874Thr)
c.11536C>A (p.Pro3846Thr)
16g.88439090C=CA2241074247ZNF469c.11620C= (p.Pro3874=)
c.11536C= (p.Pro3846=)
16g.88439090C>GCA286388324ZNF469c.11620C>G (p.Pro3874Ala)
c.11536C>G (p.Pro3846Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439090C>TCA397130714ZNF469c.11620C>T (p.Pro3874Ser)
c.11536C>T (p.Pro3846Ser)
16g.88439091C>ACA397130716ZNF469c.11621C>A (p.Pro3874Gln)
c.11537C>A (p.Pro3846Gln)
16g.88439091C>GCA397130719ZNF469c.11621C>G (p.Pro3874Arg)
c.11537C>G (p.Pro3846Arg)
16g.88439091C>TCA397130717ZNF469c.11621C>T (p.Pro3874Leu)
c.11537C>T (p.Pro3846Leu)
16g.88439092A=CA2241074250ZNF469c.11622A= (p.Pro3874=)
c.11538A= (p.Pro3846=)
16g.88439092A>CCA497359532ZNF469c.11622A>C (p.Pro3874=)
c.11538A>C (p.Pro3846=)
16g.88439092A>GCA286388348ZNF469c.11622A>G (p.Pro3874=)
c.11538A>G (p.Pro3846=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439092A>TCA497359533ZNF469c.11622A>T (p.Pro3874=)
c.11538A>T (p.Pro3846=)
16g.88439092_88439098delinsATCAGAGCA2241074252ZNF469c.11622_11628delinsATCAGAG (p.Pro3874=)
c.11538_11544delinsATCAGAG (p.Pro3846=)
16g.88439093T>ACA397130720ZNF469c.11623T>A (p.Ser3875Thr)
c.11539T>A (p.Ser3847Thr)
16g.88439093T>CCA397130722ZNF469c.11623T>C (p.Ser3875Pro)
c.11539T>C (p.Ser3847Pro)
gnomAD v4
16g.88439093T>GCA397130731ZNF469c.11623T>G (p.Ser3875Ala)
c.11539T>G (p.Ser3847Ala)
16g.88439093_88439098delCA624447643ZNF469c.11623_11628del (p.Ser3875_Glu3876del)
c.11539_11544del (p.Ser3847_Glu3848del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439094C>ACA397130733ZNF469c.11624C>A (p.Ser3875Ter)
c.11540C>A (p.Ser3847Ter)
16g.88439094C>GCA397130734ZNF469c.11624C>G (p.Ser3875Ter)
c.11540C>G (p.Ser3847Ter)
16g.88439094C>TCA397130735ZNF469c.11624C>T (p.Ser3875Leu)
c.11540C>T (p.Ser3847Leu)
16g.88439095A>CCA497359534ZNF469c.11625A>C (p.Ser3875=)
c.11541A>C (p.Ser3847=)
16g.88439095A>GCA497359535ZNF469c.11625A>G (p.Ser3875=)
c.11541A>G (p.Ser3847=)
16g.88439095A>TCA497359536ZNF469c.11625A>T (p.Ser3875=)
c.11541A>T (p.Ser3847=)
16g.88439096G>ACA397130737ZNF469c.11626G>A (p.Glu3876Lys)
c.11542G>A (p.Glu3848Lys)
16g.88439096G>CCA397130738ZNF469c.11626G>C (p.Glu3876Gln)
c.11542G>C (p.Glu3848Gln)
16g.88439096G>TCA397130740ZNF469c.11626G>T (p.Glu3876Ter)
c.11542G>T (p.Glu3848Ter)
16g.88439097A>CCA397130744ZNF469c.11627A>C (p.Glu3876Ala)
c.11543A>C (p.Glu3848Ala)
16g.88439097A>GCA397130743ZNF469c.11627A>G (p.Glu3876Gly)
c.11543A>G (p.Glu3848Gly)
16g.88439097A>TCA397130742ZNF469c.11627A>T (p.Glu3876Val)
c.11543A>T (p.Glu3848Val)
16g.88439098G>ACA497359537ZNF469c.11628G>A (p.Glu3876=)
c.11544G>A (p.Glu3848=)
ClinVar gnomAD v4
16g.88439098G>CCA397130746ZNF469c.11628G>C (p.Glu3876Asp)
c.11544G>C (p.Glu3848Asp)
16g.88439098G=CA2241074255ZNF469c.11628G= (p.Glu3876=)
c.11544G= (p.Glu3848=)
16g.88439098G>TCA397130748ZNF469c.11628G>T (p.Glu3876Asp)
c.11544G>T (p.Glu3848Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439099C>ACA397130750ZNF469c.11629C>A (p.Gln3877Lys)
c.11545C>A (p.Gln3849Lys)
16g.88439099C=CA2241074258ZNF469c.11629C= (p.Gln3877=)
c.11545C= (p.Gln3849=)
16g.88439099C>GCA397130751ZNF469c.11629C>G (p.Gln3877Glu)
c.11545C>G (p.Gln3849Glu)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439099C>TCA397130752ZNF469c.11629C>T (p.Gln3877Ter)
c.11545C>T (p.Gln3849Ter)
ClinVar gnomAD v4
16g.88439100A=CA2241074261ZNF469c.11630A= (p.Gln3877=)
c.11546A= (p.Gln3849=)
16g.88439100A>CCA397130754ZNF469c.11630A>C (p.Gln3877Pro)
c.11546A>C (p.Gln3849Pro)
16g.88439100A>GCA397130755ZNF469c.11630A>G (p.Gln3877Arg)
c.11546A>G (p.Gln3849Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439100A>TCA397130757ZNF469c.11630A>T (p.Gln3877Leu)
c.11546A>T (p.Gln3849Leu)
16g.88439101G>ACA497359538ZNF469c.11631G>A (p.Gln3877=)
c.11547G>A (p.Gln3849=)
ClinVar
16g.88439101G>CCA397130759ZNF469c.11631G>C (p.Gln3877His)
c.11547G>C (p.Gln3849His)
16g.88439101G>TCA397130761ZNF469c.11631G>T (p.Gln3877His)
c.11547G>T (p.Gln3849His)
16g.88439102C>ACA497359539ZNF469c.11632C>A (p.Arg3878=)
c.11548C>A (p.Arg3850=)
gnomAD v4
16g.88439102C=CA2241074264ZNF469c.11632C= (p.Arg3878=)
c.11548C= (p.Arg3850=)
16g.88439102C>GCA8225630ZNF469c.11632C>G (p.Arg3878Gly)
c.11548C>G (p.Arg3850Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439102C>TCA397130762ZNF469c.11632C>T (p.Arg3878Trp)
c.11548C>T (p.Arg3850Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439103G>ACA8225631ZNF469c.11633G>A (p.Arg3878Gln)
c.11549G>A (p.Arg3850Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439103G>CCA397130763ZNF469c.11633G>C (p.Arg3878Pro)
c.11549G>C (p.Arg3850Pro)
ClinVar
16g.88439103G=CA2241074268ZNF469c.11633G= (p.Arg3878=)
c.11549G= (p.Arg3850=)
16g.88439103G>TCA397130765ZNF469c.11633G>T (p.Arg3878Leu)
c.11549G>T (p.Arg3850Leu)
gnomAD v4
16g.88439104G>ACA497359540ZNF469c.11634G>A (p.Arg3878=)
c.11550G>A (p.Arg3850=)
16g.88439104G>CCA497359541ZNF469c.11634G>C (p.Arg3878=)
c.11550G>C (p.Arg3850=)
16g.88439104G>TCA497359542ZNF469c.11634G>T (p.Arg3878=)
c.11550G>T (p.Arg3850=)
16g.88439105A>CCA397130767ZNF469c.11635A>C (p.Lys3879Gln)
c.11551A>C (p.Lys3851Gln)
16g.88439105A>GCA397130768ZNF469c.11635A>G (p.Lys3879Glu)
c.11551A>G (p.Lys3851Glu)
16g.88439105A>TCA397130771ZNF469c.11635A>T (p.Lys3879Ter)
c.11551A>T (p.Lys3851Ter)
16g.88439106A>CCA397130772ZNF469c.11636A>C (p.Lys3879Thr)
c.11552A>C (p.Lys3851Thr)
16g.88439106A>GCA397130773ZNF469c.11636A>G (p.Lys3879Arg)
c.11552A>G (p.Lys3851Arg)
16g.88439106A>TCA397130774ZNF469c.11636A>T (p.Lys3879Met)
c.11552A>T (p.Lys3851Met)
16g.88439107G>ACA286388354ZNF469c.11637G>A (p.Lys3879=)
c.11553G>A (p.Lys3851=)
ClinVar dbSNP gnomAD v4
16g.88439107G>CCA397130776ZNF469c.11637G>C (p.Lys3879Asn)
c.11553G>C (p.Lys3851Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439107G=CA2241074271ZNF469c.11637G= (p.Lys3879=)
c.11553G= (p.Lys3851=)
16g.88439107G>TCA397130778ZNF469c.11637G>T (p.Lys3879Asn)
c.11553G>T (p.Lys3851Asn)
16g.88439108G>ACA397130780ZNF469c.11638G>A (p.Ala3880Thr)
c.11554G>A (p.Ala3852Thr)
dbSNP gnomAD v4
16g.88439108G>CCA397130781ZNF469c.11638G>C (p.Ala3880Pro)
c.11554G>C (p.Ala3852Pro)
16g.88439108G=CA2241074274ZNF469c.11638G= (p.Ala3880=)
c.11554G= (p.Ala3852=)
16g.88439108G>TCA397130787ZNF469c.11638G>T (p.Ala3880Ser)
c.11554G>T (p.Ala3852Ser)
16g.88439109C>ACA397130790ZNF469c.11639C>A (p.Ala3880Glu)
c.11555C>A (p.Ala3852Glu)
16g.88439109C=CA2241074277ZNF469c.11639C= (p.Ala3880=)
c.11555C= (p.Ala3852=)
16g.88439109C>GCA397130792ZNF469c.11639C>G (p.Ala3880Gly)
c.11555C>G (p.Ala3852Gly)
16g.88439109C>TCA397130789ZNF469c.11639C>T (p.Ala3880Val)
c.11555C>T (p.Ala3852Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439110A=CA2241074280ZNF469c.11640A= (p.Ala3880=)
c.11556A= (p.Ala3852=)
16g.88439110A>CCA497359543ZNF469c.11640A>C (p.Ala3880=)
c.11556A>C (p.Ala3852=)
dbSNP
16g.88439110A>GCA497359544ZNF469c.11640A>G (p.Ala3880=)
c.11556A>G (p.Ala3852=)
gnomAD v4
16g.88439110A>TCA497359545ZNF469c.11640A>T (p.Ala3880=)
c.11556A>T (p.Ala3852=)
16g.88439111G>ACA397130793ZNF469c.11641G>A (p.Glu3881Lys)
c.11557G>A (p.Glu3853Lys)
16g.88439111G>CCA397130795ZNF469c.11641G>C (p.Glu3881Gln)
c.11557G>C (p.Glu3853Gln)
dbSNP
16g.88439111G=CA2241074282ZNF469c.11641G= (p.Glu3881=)
c.11557G= (p.Glu3853=)
16g.88439111G>TCA397130796ZNF469c.11641G>T (p.Glu3881Ter)
c.11557G>T (p.Glu3853Ter)
gnomAD v4
16g.88439112A>CCA397130798ZNF469c.11642A>C (p.Glu3881Ala)
c.11558A>C (p.Glu3853Ala)
16g.88439112A>GCA397130800ZNF469c.11642A>G (p.Glu3881Gly)
c.11558A>G (p.Glu3853Gly)
16g.88439112A>TCA397130804ZNF469c.11642A>T (p.Glu3881Val)
c.11558A>T (p.Glu3853Val)
16g.88439113G>ACA497359546ZNF469c.11643G>A (p.Glu3881=)
c.11559G>A (p.Glu3853=)
16g.88439113G>CCA397130805ZNF469c.11643G>C (p.Glu3881Asp)
c.11559G>C (p.Glu3853Asp)
16g.88439113G>TCA397130807ZNF469c.11643G>T (p.Glu3881Asp)
c.11559G>T (p.Glu3853Asp)
gnomAD v4
16g.88439114C>ACA397130808ZNF469c.11644C>A (p.Pro3882Thr)
c.11560C>A (p.Pro3854Thr)
16g.88439114C=CA2241074285ZNF469c.11644C= (p.Pro3882=)
c.11560C= (p.Pro3854=)
16g.88439114C>GCA397130810ZNF469c.11644C>G (p.Pro3882Ala)
c.11560C>G (p.Pro3854Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88439114C>TCA397130812ZNF469c.11644C>T (p.Pro3882Ser)
c.11560C>T (p.Pro3854Ser)
dbSNP
16g.88439115C>ACA397130813ZNF469c.11645C>A (p.Pro3882Gln)
c.11561C>A (p.Pro3854Gln)
gnomAD v4
16g.88439115C=CA2241074289ZNF469c.11645C= (p.Pro3882=)
c.11561C= (p.Pro3854=)
16g.88439115C>GCA397130814ZNF469c.11645C>G (p.Pro3882Arg)
c.11561C>G (p.Pro3854Arg)
dbSNP gnomAD v2 gnomAD v4
16g.88439115C>TCA8225632ZNF469c.11645C>T (p.Pro3882Leu)
c.11561C>T (p.Pro3854Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439116G>ACA8225633ZNF469c.11646G>A (p.Pro3882=)
c.11562G>A (p.Pro3854=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439116G>CCA286388361ZNF469c.11646G>C (p.Pro3882=)
c.11562G>C (p.Pro3854=)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88439116G=CA2241074296ZNF469c.11646G= (p.Pro3882=)
c.11562G= (p.Pro3854=)
16g.88439116G>TCA497359547ZNF469c.11646G>T (p.Pro3882=)
c.11562G>T (p.Pro3854=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439117G>ACA397130818ZNF469c.11647G>A (p.Gly3883Ser)
c.11563G>A (p.Gly3855Ser)
16g.88439117G>CCA397130819ZNF469c.11647G>C (p.Gly3883Arg)
c.11563G>C (p.Gly3855Arg)
16g.88439117G>TCA397130821ZNF469c.11647G>T (p.Gly3883Cys)
c.11563G>T (p.Gly3855Cys)
16g.88439118G>ACA397130823ZNF469c.11648G>A (p.Gly3883Asp)
c.11564G>A (p.Gly3855Asp)
16g.88439118G>CCA397130824ZNF469c.11648G>C (p.Gly3883Ala)
c.11564G>C (p.Gly3855Ala)
16g.88439118G>TCA397130826ZNF469c.11648G>T (p.Gly3883Val)
c.11564G>T (p.Gly3855Val)
16g.88439119C>ACA497359550ZNF469c.11649C>A (p.Gly3883=)
c.11565C>A (p.Gly3855=)
ClinVar gnomAD v4
16g.88439119C>GCA497359549ZNF469c.11649C>G (p.Gly3883=)
c.11565C>G (p.Gly3855=)
16g.88439119C>TCA497359548ZNF469c.11649C>T (p.Gly3883=)
c.11565C>T (p.Gly3855=)
ClinVar dbSNP gnomAD v4
16g.88439120C>ACA397130829ZNF469c.11650C>A (p.His3884Asn)
c.11566C>A (p.His3856Asn)
16g.88439120C>GCA397130830ZNF469c.11650C>G (p.His3884Asp)
c.11566C>G (p.His3856Asp)
16g.88439120C>TCA397130832ZNF469c.11650C>T (p.His3884Tyr)
c.11566C>T (p.His3856Tyr)
16g.88439121A>CCA397130833ZNF469c.11651A>C (p.His3884Pro)
c.11567A>C (p.His3856Pro)
16g.88439121A>GCA397130834ZNF469c.11651A>G (p.His3884Arg)
c.11567A>G (p.His3856Arg)
16g.88439121A>TCA397130835ZNF469c.11651A>T (p.His3884Leu)
c.11567A>T (p.His3856Leu)
16g.88439122C>ACA397130836ZNF469c.11652C>A (p.His3884Gln)
c.11568C>A (p.His3856Gln)
16g.88439122C>GCA397130837ZNF469c.11652C>G (p.His3884Gln)
c.11568C>G (p.His3856Gln)
16g.88439122C>TCA497359551ZNF469c.11652C>T (p.His3884=)
c.11568C>T (p.His3856=)
16g.88439123A>CCA397130838ZNF469c.11653A>C (p.Thr3885Pro)
c.11569A>C (p.Thr3857Pro)
16g.88439123A>GCA397130842ZNF469c.11653A>G (p.Thr3885Ala)
c.11569A>G (p.Thr3857Ala)
16g.88439123A>TCA397130840ZNF469c.11653A>T (p.Thr3885Ser)
c.11569A>T (p.Thr3857Ser)
16g.88439124C>ACA397130843ZNF469c.11654C>A (p.Thr3885Lys)
c.11570C>A (p.Thr3857Lys)
dbSNP
16g.88439124C=CA2241074299ZNF469c.11654C= (p.Thr3885=)
c.11570C= (p.Thr3857=)
16g.88439124C>GCA397130844ZNF469c.11654C>G (p.Thr3885Arg)
c.11570C>G (p.Thr3857Arg)
16g.88439124C>TCA286388362ZNF469c.11654C>T (p.Thr3885Ile)
c.11570C>T (p.Thr3857Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439125A>CCA497359554ZNF469c.11655A>C (p.Thr3885=)
c.11571A>C (p.Thr3857=)
16g.88439125A>GCA497359555ZNF469c.11655A>G (p.Thr3885=)
c.11571A>G (p.Thr3857=)
ClinVar gnomAD v4
16g.88439125A>TCA497359556ZNF469c.11655A>T (p.Thr3885=)
c.11571A>T (p.Thr3857=)
16g.88439126C>ACA397130847ZNF469c.11656C>A (p.Gln3886Lys)
c.11572C>A (p.Gln3858Lys)
16g.88439126C>GCA397130849ZNF469c.11656C>G (p.Gln3886Glu)
c.11572C>G (p.Gln3858Glu)
16g.88439126C>TCA397130850ZNF469c.11656C>T (p.Gln3886Ter)
c.11572C>T (p.Gln3858Ter)
16g.88439126_88439128delinsCAGCA2241074301ZNF469c.11656_11658delinsCAG (p.Gln3886=)
c.11572_11574delinsCAG (p.Gln3858=)
16g.88439127A=CA2241074306ZNF469c.11657A= (p.Gln3886=)
c.11573A= (p.Gln3858=)
16g.88439127A>CCA397130852ZNF469c.11657A>C (p.Gln3886Pro)
c.11573A>C (p.Gln3858Pro)
16g.88439127A>GCA397130854ZNF469c.11657A>G (p.Gln3886Arg)
c.11573A>G (p.Gln3858Arg)
dbSNP gnomAD v2 gnomAD v4
16g.88439127A>TCA397130856ZNF469c.11657A>T (p.Gln3886Leu)
c.11573A>T (p.Gln3858Leu)
dbSNP
16g.88439129_88439130delCA2241074303ZNF469c.11659_11660del (p.Arg3887GlufsTer28)
c.11575_11576del (p.Arg3859GlufsTer28)
dbSNP gnomAD v4
16g.88439128G>ACA497359560ZNF469c.11658G>A (p.Gln3886=)
c.11574G>A (p.Gln3858=)
16g.88439128G>CCA8225634ZNF469c.11658G>C (p.Gln3886His)
c.11574G>C (p.Gln3858His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439128G=CA2241074309ZNF469c.11658G= (p.Gln3886=)
c.11574G= (p.Gln3858=)
16g.88439128G>TCA397130858ZNF469c.11658G>T (p.Gln3886His)
c.11574G>T (p.Gln3858His)
16g.88439128_88439129insTCA286388365ZNF469c.11658_11659insT (p.Arg3887Ter)
c.11574_11575insT (p.Arg3859Ter)
dbSNP
16g.88439129A=CA2241074312ZNF469c.11659A= (p.Arg3887=)
c.11575A= (p.Arg3859=)
16g.88439129A>CCA497359562ZNF469c.11659A>C (p.Arg3887=)
c.11575A>C (p.Arg3859=)
16g.88439129A>GCA397130861ZNF469c.11659A>G (p.Arg3887Gly)
c.11575A>G (p.Arg3859Gly)
gnomAD v4
16g.88439129A>TCA397130860ZNF469c.11659A>T (p.Arg3887Trp)
c.11575A>T (p.Arg3859Trp)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88439130G>ACA397130863ZNF469c.11660G>A (p.Arg3887Lys)
c.11576G>A (p.Arg3859Lys)
gnomAD v4
16g.88439130G>CCA397130865ZNF469c.11660G>C (p.Arg3887Thr)
c.11576G>C (p.Arg3859Thr)
16g.88439130G>TCA397130867ZNF469c.11660G>T (p.Arg3887Met)
c.11576G>T (p.Arg3859Met)
16g.88439131G>ACA497359563ZNF469c.11661G>A (p.Arg3887=)
c.11577G>A (p.Arg3859=)
dbSNP gnomAD v2 gnomAD v4
16g.88439131G>CCA397130869ZNF469c.11661G>C (p.Arg3887Ser)
c.11577G>C (p.Arg3859Ser)
16g.88439131G=CA2241074313ZNF469c.11661G= (p.Arg3887=)
c.11577G= (p.Arg3859=)
16g.88439131G>TCA397130875ZNF469c.11661G>T (p.Arg3887Ser)
c.11577G>T (p.Arg3859Ser)
16g.88439132A>CCA397130876ZNF469c.11662A>C (p.Lys3888Gln)
c.11578A>C (p.Lys3860Gln)
16g.88439132A>GCA397130878ZNF469c.11662A>G (p.Lys3888Glu)
c.11578A>G (p.Lys3860Glu)
16g.88439132A>TCA397130880ZNF469c.11662A>T (p.Lys3888Ter)
c.11578A>T (p.Lys3860Ter)
16g.88439133A>CCA397130881ZNF469c.11663A>C (p.Lys3888Thr)
c.11579A>C (p.Lys3860Thr)
16g.88439133A>GCA397130883ZNF469c.11663A>G (p.Lys3888Arg)
c.11579A>G (p.Lys3860Arg)
gnomAD v4
16g.88439133A>TCA397130884ZNF469c.11663A>T (p.Lys3888Met)
c.11579A>T (p.Lys3860Met)
16g.88439134G>ACA497359565ZNF469c.11664G>A (p.Lys3888=)
c.11580G>A (p.Lys3860=)
gnomAD v4
16g.88439134G>CCA397130886ZNF469c.11664G>C (p.Lys3888Asn)
c.11580G>C (p.Lys3860Asn)
16g.88439134G>TCA397130889ZNF469c.11664G>T (p.Lys3888Asn)
c.11580G>T (p.Lys3860Asn)
16g.88439135G>ACA397130892ZNF469c.11665G>A (p.Asp3889Asn)
c.11581G>A (p.Asp3861Asn)
dbSNP gnomAD v3 gnomAD v4
16g.88439135G>CCA397130894ZNF469c.11665G>C (p.Asp3889His)
c.11581G>C (p.Asp3861His)
16g.88439135G=CA2241074316ZNF469c.11665G= (p.Asp3889=)
c.11581G= (p.Asp3861=)
16g.88439135G>TCA397130891ZNF469c.11665G>T (p.Asp3889Tyr)
c.11581G>T (p.Asp3861Tyr)
gnomAD v4
16g.88439136A=CA2241074319ZNF469c.11666A= (p.Asp3889=)
c.11582A= (p.Asp3861=)
16g.88439136A>CCA397130897ZNF469c.11666A>C (p.Asp3889Ala)
c.11582A>C (p.Asp3861Ala)
16g.88439136A>GCA397130895ZNF469c.11666A>G (p.Asp3889Gly)
c.11582A>G (p.Asp3861Gly)
dbSNP gnomAD v3 gnomAD v4
16g.88439136A>TCA397130898ZNF469c.11666A>T (p.Asp3889Val)
c.11582A>T (p.Asp3861Val)
16g.88439137C>ACA397130900ZNF469c.11667C>A (p.Asp3889Glu)
c.11583C>A (p.Asp3861Glu)
16g.88439137C=CA2241074322ZNF469c.11667C= (p.Asp3889=)
c.11583C= (p.Asp3861=)
16g.88439137C>GCA397130901ZNF469c.11667C>G (p.Asp3889Glu)
c.11583C>G (p.Asp3861Glu)
16g.88439137C>TCA497359568ZNF469c.11667C>T (p.Asp3889=)
c.11583C>T (p.Asp3861=)
dbSNP gnomAD v2
16g.88439138A>CCA497359569ZNF469c.11668A>C (p.Arg3890=)
c.11584A>C (p.Arg3862=)
16g.88439138A>GCA397130903ZNF469c.11668A>G (p.Arg3890Gly)
c.11584A>G (p.Arg3862Gly)
16g.88439138A>TCA397130905ZNF469c.11668A>T (p.Arg3890Ter)
c.11584A>T (p.Arg3862Ter)
16g.88439139G>ACA397130907ZNF469c.11669G>A (p.Arg3890Lys)
c.11585G>A (p.Arg3862Lys)
gnomAD v4
16g.88439139G>CCA397130910ZNF469c.11669G>C (p.Arg3890Thr)
c.11585G>C (p.Arg3862Thr)
dbSNP
16g.88439139G=CA2241074323ZNF469c.11669G= (p.Arg3890=)
c.11585G= (p.Arg3862=)
16g.88439139G>TCA397130911ZNF469c.11669G>T (p.Arg3890Ile)
c.11585G>T (p.Arg3862Ile)
16g.88439140A=CA2241074325ZNF469c.11670A= (p.Arg3890=)
c.11586A= (p.Arg3862=)
16g.88439140A>CCA397130912ZNF469c.11670A>C (p.Arg3890Ser)
c.11586A>C (p.Arg3862Ser)
16g.88439140A>GCA497359571ZNF469c.11670A>G (p.Arg3890=)
c.11586A>G (p.Arg3862=)
ClinVar dbSNP gnomAD v4
16g.88439140A>TCA397130914ZNF469c.11670A>T (p.Arg3890Ser)
c.11586A>T (p.Arg3862Ser)
16g.88439141C>ACA397130918ZNF469c.11671C>A (p.Leu3891Met)
c.11587C>A (p.Leu3863Met)
dbSNP gnomAD v2
16g.88439141C=CA2241074328ZNF469c.11671C= (p.Leu3891=)
c.11587C= (p.Leu3863=)
16g.88439141C>GCA397130921ZNF469c.11671C>G (p.Leu3891Val)
c.11587C>G (p.Leu3863Val)
ClinVar dbSNP gnomAD v4
16g.88439141C>TCA497359574ZNF469c.11671C>T (p.Leu3891=)
c.11587C>T (p.Leu3863=)
16g.88439142T>ACA397130926ZNF469c.11672T>A (p.Leu3891Gln)
c.11588T>A (p.Leu3863Gln)
gnomAD v4
16g.88439142T>CCA397130924ZNF469c.11672T>C (p.Leu3891Pro)
c.11588T>C (p.Leu3863Pro)
16g.88439142T>GCA397130923ZNF469c.11672T>G (p.Leu3891Arg)
c.11588T>G (p.Leu3863Arg)
16g.88439142dupCA2576089665ZNF469c.11672dup (p.Lys3893GlnfsTer23)
c.11588dup (p.Lys3865GlnfsTer23)
16g.88439143G>ACA497359576ZNF469c.11673G>A (p.Leu3891=)
c.11589G>A (p.Leu3863=)
ClinVar dbSNP gnomAD v4
16g.88439143G>CCA497359577ZNF469c.11673G>C (p.Leu3891=)
c.11589G>C (p.Leu3863=)
16g.88439143G=CA2241074329ZNF469c.11673G= (p.Leu3891=)
c.11589G= (p.Leu3863=)
16g.88439143G>TCA497359578ZNF469c.11673G>T (p.Leu3891=)
c.11589G>T (p.Leu3863=)
ClinVar
16g.88439144G>ACA397130928ZNF469c.11674G>A (p.Gly3892Ser)
c.11590G>A (p.Gly3864Ser)
16g.88439144G>CCA397130929ZNF469c.11674G>C (p.Gly3892Arg)
c.11590G>C (p.Gly3864Arg)
16g.88439144G>TCA397130931ZNF469c.11674G>T (p.Gly3892Cys)
c.11590G>T (p.Gly3864Cys)
gnomAD v4
16g.88439145G>ACA397130934ZNF469c.11675G>A (p.Gly3892Asp)
c.11591G>A (p.Gly3864Asp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439145G>CCA397130935ZNF469c.11675G>C (p.Gly3892Ala)
c.11591G>C (p.Gly3864Ala)
16g.88439145G=CA2241074330ZNF469c.11675G= (p.Gly3892=)
c.11591G= (p.Gly3864=)
16g.88439145G>TCA397130937ZNF469c.11675G>T (p.Gly3892Val)
c.11591G>T (p.Gly3864Val)
16g.88439146C>ACA286388370ZNF469c.11676C>A (p.Gly3892=)
c.11592C>A (p.Gly3864=)
ClinVar dbSNP
16g.88439146C=CA2241074333ZNF469c.11676C= (p.Gly3892=)
c.11592C= (p.Gly3864=)
16g.88439146C>GCA497359581ZNF469c.11676C>G (p.Gly3892=)
c.11592C>G (p.Gly3864=)
16g.88439146C>TCA497359580ZNF469c.11676C>T (p.Gly3892=)
c.11592C>T (p.Gly3864=)
gnomAD v4
16g.88439147A>CCA397130938ZNF469c.11677A>C (p.Lys3893Gln)
c.11593A>C (p.Lys3865Gln)
16g.88439147A>GCA397130939ZNF469c.11677A>G (p.Lys3893Glu)
c.11593A>G (p.Lys3865Glu)
16g.88439147A>TCA397130940ZNF469c.11677A>T (p.Lys3893Ter)
c.11593A>T (p.Lys3865Ter)
16g.88439148A=CA2241074334ZNF469c.11678A= (p.Lys3893=)
c.11594A= (p.Lys3865=)
16g.88439148A>CCA397130941ZNF469c.11678A>C (p.Lys3893Thr)
c.11594A>C (p.Lys3865Thr)
16g.88439148A>GCA397130943ZNF469c.11678A>G (p.Lys3893Arg)
c.11594A>G (p.Lys3865Arg)
16g.88439148A>TCA286388380ZNF469c.11678A>T (p.Lys3893Met)
c.11594A>T (p.Lys3865Met)
dbSNP gnomAD v4
16g.88439149G>ACA497359583ZNF469c.11679G>A (p.Lys3893=)
c.11595G>A (p.Lys3865=)
16g.88439149G>CCA397130948ZNF469c.11679G>C (p.Lys3893Asn)
c.11595G>C (p.Lys3865Asn)
16g.88439149G>TCA397130946ZNF469c.11679G>T (p.Lys3893Asn)
c.11595G>T (p.Lys3865Asn)
gnomAD v4
16g.88439150G>ACA397130949ZNF469c.11680G>A (p.Ala3894Thr)
c.11596G>A (p.Ala3866Thr)
ClinVar dbSNP gnomAD v4
16g.88439150G>CCA286388387ZNF469c.11680G>C (p.Ala3894Pro)
c.11596G>C (p.Ala3866Pro)
dbSNP
16g.88439150G=CA2241074336ZNF469c.11680G= (p.Ala3894=)
c.11596G= (p.Ala3866=)
16g.88439150G>TCA397130951ZNF469c.11680G>T (p.Ala3894Ser)
c.11596G>T (p.Ala3866Ser)
gnomAD v4
16g.88439151C>ACA397130953ZNF469c.11681C>A (p.Ala3894Asp)
c.11597C>A (p.Ala3866Asp)
gnomAD v4
16g.88439151C>GCA397130955ZNF469c.11681C>G (p.Ala3894Gly)
c.11597C>G (p.Ala3866Gly)
16g.88439151C>TCA397130956ZNF469c.11681C>T (p.Ala3894Val)
c.11597C>T (p.Ala3866Val)
ClinVar
16g.88439152C>ACA497359584ZNF469c.11682C>A (p.Ala3894=)
c.11598C>A (p.Ala3866=)
16g.88439152C=CA2241074339ZNF469c.11682C= (p.Ala3894=)
c.11598C= (p.Ala3866=)
16g.88439152C>GCA497359586ZNF469c.11682C>G (p.Ala3894=)
c.11598C>G (p.Ala3866=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88439152C>TCA497359585ZNF469c.11682C>T (p.Ala3894=)
c.11598C>T (p.Ala3866=)
16g.88439153T>ACA397130961ZNF469c.11683T>A (p.Phe3895Ile)
c.11599T>A (p.Phe3867Ile)
16g.88439153T>CCA397130958ZNF469c.11683T>C (p.Phe3895Leu)
c.11599T>C (p.Phe3867Leu)
gnomAD v4
16g.88439153T>GCA397130960ZNF469c.11683T>G (p.Phe3895Val)
c.11599T>G (p.Phe3867Val)
16g.88439154T>ACA397130963ZNF469c.11684T>A (p.Phe3895Tyr)
c.11600T>A (p.Phe3867Tyr)
16g.88439154T>CCA397130964ZNF469c.11684T>C (p.Phe3895Ser)
c.11600T>C (p.Phe3867Ser)
dbSNP gnomAD v4
16g.88439154T>GCA397130965ZNF469c.11684T>G (p.Phe3895Cys)
c.11600T>G (p.Phe3867Cys)
16g.88439154T=CA2241074341ZNF469c.11684T= (p.Phe3895=)
c.11600T= (p.Phe3867=)
16g.88439155C>ACA397130967ZNF469c.11685C>A (p.Phe3895Leu)
c.11601C>A (p.Phe3867Leu)
16g.88439155C>GCA397130969ZNF469c.11685C>G (p.Phe3895Leu)
c.11601C>G (p.Phe3867Leu)
16g.88439155C>TCA497359588ZNF469c.11685C>T (p.Phe3895=)
c.11601C>T (p.Phe3867=)
16g.88439156C>ACA397130970ZNF469c.11686C>A (p.Pro3896Thr)
c.11602C>A (p.Pro3868Thr)
16g.88439156C>GCA397130974ZNF469c.11686C>G (p.Pro3896Ala)
c.11602C>G (p.Pro3868Ala)
16g.88439156C>TCA397130972ZNF469c.11686C>T (p.Pro3896Ser)
c.11602C>T (p.Pro3868Ser)
COSMIC
16g.88439157C>ACA397130976ZNF469c.11687C>A (p.Pro3896His)
c.11603C>A (p.Pro3868His)
16g.88439157C>GCA397130977ZNF469c.11687C>G (p.Pro3896Arg)
c.11603C>G (p.Pro3868Arg)
16g.88439157C>TCA397130978ZNF469c.11687C>T (p.Pro3896Leu)
c.11603C>T (p.Pro3868Leu)
16g.88439158C>ACA497359589ZNF469c.11688C>A (p.Pro3896=)
c.11604C>A (p.Pro3868=)
COSMIC
16g.88439158C=CA2241074343ZNF469c.11688C= (p.Pro3896=)
c.11604C= (p.Pro3868=)
16g.88439158C>GCA497359590ZNF469c.11688C>G (p.Pro3896=)
c.11604C>G (p.Pro3868=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439158C>TCA497359591ZNF469c.11688C>T (p.Pro3896=)
c.11604C>T (p.Pro3868=)
16g.88439159C>ACA397130980ZNF469c.11689C>A (p.Gln3897Lys)
c.11605C>A (p.Gln3869Lys)
16g.88439159C=CA2241074347ZNF469c.11689C= (p.Gln3897=)
c.11605C= (p.Gln3869=)
16g.88439159C>GCA397130982ZNF469c.11689C>G (p.Gln3897Glu)
c.11605C>G (p.Gln3869Glu)
gnomAD v4
16g.88439159C>TCA397130983ZNF469c.11689C>T (p.Gln3897Ter)
c.11605C>T (p.Gln3869Ter)
16g.88439159_88439160delinsCACA2241074349ZNF469c.11689_11690delinsCA (p.Gln3897=)
c.11605_11606delinsCA (p.Gln3869=)
16g.88439160delCA2241074354ZNF469c.11690del (p.Gln3897ArgfsTer?)
c.11606del (p.Gln3869ArgfsTer?)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88439160A=CA2241074356ZNF469c.11690A= (p.Gln3897=)
c.11606A= (p.Gln3869=)
16g.88439160A>CCA397130985ZNF469c.11690A>C (p.Gln3897Pro)
c.11606A>C (p.Gln3869Pro)
16g.88439160A>GCA397130986ZNF469c.11690A>G (p.Gln3897Arg)
c.11606A>G (p.Gln3869Arg)
dbSNP gnomAD v4
16g.88439160A>TCA397130988ZNF469c.11690A>T (p.Gln3897Leu)
c.11606A>T (p.Gln3869Leu)
ClinVar
16g.88439160dupCA725571455ZNF469c.11690dup (p.Arg3899GlufsTer17)
c.11606dup (p.Arg3871GlufsTer17)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.88439161G>ACA497359592ZNF469c.11691G>A (p.Gln3897=)
c.11607G>A (p.Gln3869=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439161G>CCA397130990ZNF469c.11691G>C (p.Gln3897His)
c.11607G>C (p.Gln3869His)
gnomAD v4
16g.88439161G=CA2241074361ZNF469c.11691G= (p.Gln3897=)
c.11607G= (p.Gln3869=)
16g.88439161G>TCA397130991ZNF469c.11691G>T (p.Gln3897His)
c.11607G>T (p.Gln3869His)
16g.88439162G>ACA397130995ZNF469c.11692G>A (p.Gly3898Arg)
c.11608G>A (p.Gly3870Arg)
dbSNP
16g.88439162G>CCA397130997ZNF469c.11692G>C (p.Gly3898Arg)
c.11608G>C (p.Gly3870Arg)
gnomAD v4
16g.88439162G=CA2241074365ZNF469c.11692G= (p.Gly3898=)
c.11608G= (p.Gly3870=)
16g.88439162G>TCA397130993ZNF469c.11692G>T (p.Gly3898Trp)
c.11608G>T (p.Gly3870Trp)
16g.88439163G>ACA397131001ZNF469c.11693G>A (p.Gly3898Glu)
c.11609G>A (p.Gly3870Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88439163G>CCA397130998ZNF469c.11693G>C (p.Gly3898Ala)
c.11609G>C (p.Gly3870Ala)
16g.88439163G=CA2241074368ZNF469c.11693G= (p.Gly3898=)
c.11609G= (p.Gly3870=)
16g.88439163G>TCA397130999ZNF469c.11693G>T (p.Gly3898Val)
c.11609G>T (p.Gly3870Val)
16g.88439164G>ACA497359595ZNF469c.11694G>A (p.Gly3898=)
c.11610G>A (p.Gly3870=)
dbSNP gnomAD v3 gnomAD v4
16g.88439164G>CCA497359596ZNF469c.11694G>C (p.Gly3898=)
c.11610G>C (p.Gly3870=)
16g.88439164G=CA2241074371ZNF469c.11694G= (p.Gly3898=)
c.11610G= (p.Gly3870=)
16g.88439164G>TCA497359597ZNF469c.11694G>T (p.Gly3898=)
c.11610G>T (p.Gly3870=)
gnomAD v4
16g.88439165A=CA2241074374ZNF469c.11695A= (p.Arg3899=)
c.11611A= (p.Arg3871=)
16g.88439165A>CCA497359598ZNF469c.11695A>C (p.Arg3899=)
c.11611A>C (p.Arg3871=)
16g.88439165A>GCA397131002ZNF469c.11695A>G (p.Arg3899Gly)
c.11611A>G (p.Arg3871Gly)
16g.88439165A>TCA397131003ZNF469c.11695A>T (p.Arg3899Ter)
c.11611A>T (p.Arg3871Ter)
dbSNP gnomAD v3 gnomAD v4
16g.88439166G>ACA397131004ZNF469c.11696G>A (p.Arg3899Lys)
c.11612G>A (p.Arg3871Lys)
gnomAD v4
16g.88439166G>CCA397131006ZNF469c.11696G>C (p.Arg3899Thr)
c.11612G>C (p.Arg3871Thr)
16g.88439166G>TCA397131007ZNF469c.11696G>T (p.Arg3899Ile)
c.11612G>T (p.Arg3871Ile)
gnomAD v4
16g.88439167A=CA2241074375ZNF469c.11697A= (p.Arg3899=)
c.11613A= (p.Arg3871=)
16g.88439167A>CCA8225635ZNF469c.11697A>C (p.Arg3899Ser)
c.11613A>C (p.Arg3871Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88439167A>GCA497359599ZNF469c.11697A>G (p.Arg3899=)
c.11613A>G (p.Arg3871=)
16g.88439167A>TCA397131009ZNF469c.11697A>T (p.Arg3899Ser)
c.11613A>T (p.Arg3871Ser)
16g.88439168C>ACA397131010ZNF469c.11698C>A (p.Pro3900Thr)
c.11614C>A (p.Pro3872Thr)
dbSNP gnomAD v2 gnomAD v4
16g.88439168C=CA2241074379ZNF469c.11698C= (p.Pro3900=)
c.11614C= (p.Pro3872=)
16g.88439168C>GCA397131011ZNF469c.11698C>G (p.Pro3900Ala)
c.11614C>G (p.Pro3872Ala)
16g.88439168C>TCA397131013ZNF469c.11698C>T (p.Pro3900Ser)
c.11614C>T (p.Pro3872Ser)
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

Number of alleles fetched