Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119674392_119683124delCA2580082473 ClinVar
10g.119675031_119678711delCA2580082474 ClinVar
10g.119676533C>ACA378296392BAG3c.979C>A (p.Pro327Thr)
c.802C>A (p.Pro268Thr)
c.976C>A (p.Pro326Thr)
ClinVar dbSNP
10g.119676533C=CA1940196554BAG3c.979C= (p.Pro327=)
c.802C= (p.Pro268=)
c.976C= (p.Pro326=)
10g.119676533C>GCA378296390BAG3c.979C>G (p.Pro327Ala)
c.802C>G (p.Pro268Ala)
c.976C>G (p.Pro326Ala)
gnomAD v4
10g.119676533C>TCA378296391BAG3c.979C>T (p.Pro327Ser)
c.802C>T (p.Pro268Ser)
c.976C>T (p.Pro326Ser)
10g.119676534C>ACA378296393BAG3c.980C>A (p.Pro327Gln)
c.803C>A (p.Pro268Gln)
c.977C>A (p.Pro326Gln)
10g.119676534C=CA1940196555BAG3c.980C= (p.Pro327=)
c.803C= (p.Pro268=)
c.977C= (p.Pro326=)
10g.119676534C>GCA378296394BAG3c.980C>G (p.Pro327Arg)
c.803C>G (p.Pro268Arg)
c.977C>G (p.Pro326Arg)
ClinVar dbSNP
10g.119676534C>TCA378296395BAG3c.980C>T (p.Pro327Leu)
c.803C>T (p.Pro268Leu)
c.977C>T (p.Pro326Leu)
10g.119676535A=CA1940196556BAG3c.981A= (p.Pro327=)
c.804A= (p.Pro268=)
c.978A= (p.Pro326=)
10g.119676535A>CCA471634815BAG3c.981A>C (p.Pro327=)
c.804A>C (p.Pro268=)
c.978A>C (p.Pro326=)
10g.119676535A>GCA214224724BAG3c.981A>G (p.Pro327=)
c.804A>G (p.Pro268=)
c.978A>G (p.Pro326=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676535A>TCA471634816BAG3c.981A>T (p.Pro327=)
c.804A>T (p.Pro268=)
c.978A>T (p.Pro326=)
10g.119676535_119676538delinsAGTTCA1940196557BAG3c.981_984delinsAGTT (p.Pro327=)
c.804_807delinsAGTT (p.Pro268=)
c.978_981delinsAGTT (p.Pro326=)
10g.119676536G>ACA378296396BAG3c.982G>A (p.Val328Ile)
c.805G>A (p.Val269Ile)
c.979G>A (p.Val327Ile)
dbSNP gnomAD v2 gnomAD v4
10g.119676536G>CCA378296397BAG3c.982G>C (p.Val328Leu)
c.805G>C (p.Val269Leu)
c.979G>C (p.Val327Leu)
10g.119676536G=CA1940196558BAG3c.982G= (p.Val328=)
c.805G= (p.Val269=)
c.979G= (p.Val327=)
10g.119676536G>TCA378296398BAG3c.982G>T (p.Val328Phe)
c.805G>T (p.Val269Phe)
c.979G>T (p.Val327Phe)
10g.119676537_119676539delCA660668459BAG3c.983_985del (p.Val328del)
c.806_808del (p.Val269del)
c.980_982del (p.Val327del)
dbSNP
10g.119676537T>ACA378296399BAG3c.983T>A (p.Val328Asp)
c.806T>A (p.Val269Asp)
c.980T>A (p.Val327Asp)
gnomAD v4
10g.119676537T>CCA5716458BAG3c.983T>C (p.Val328Ala)
c.806T>C (p.Val269Ala)
c.980T>C (p.Val327Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676537T>GCA378296400BAG3c.983T>G (p.Val328Gly)
c.806T>G (p.Val269Gly)
c.980T>G (p.Val327Gly)
ClinVar dbSNP
10g.119676537T=CA1940196559BAG3c.983T= (p.Val328=)
c.806T= (p.Val269=)
c.980T= (p.Val327=)
10g.119676538T>ACA471634817BAG3c.984T>A (p.Val328=)
c.807T>A (p.Val269=)
c.981T>A (p.Val327=)
10g.119676538T>CCA471634818BAG3c.984T>C (p.Val328=)
c.807T>C (p.Val269=)
c.981T>C (p.Val327=)
10g.119676538T>GCA5716459BAG3c.984T>G (p.Val328=)
c.807T>G (p.Val269=)
c.981T>G (p.Val327=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676538T=CA1940196560BAG3c.984T= (p.Val328=)
c.807T= (p.Val269=)
c.981T= (p.Val327=)
10g.119676539G>ACA378296401BAG3c.985G>A (p.Gly329Arg)
c.808G>A (p.Gly270Arg)
c.982G>A (p.Gly328Arg)
10g.119676539G>CCA378296402BAG3c.985G>C (p.Gly329Arg)
c.808G>C (p.Gly270Arg)
c.982G>C (p.Gly328Arg)
10g.119676539G>TCA378296403BAG3c.985G>T (p.Gly329Ter)
c.808G>T (p.Gly270Ter)
c.982G>T (p.Gly328Ter)
COSMIC
10g.119676540G>ACA214224738BAG3c.986G>A (p.Gly329Glu)
c.809G>A (p.Gly270Glu)
c.983G>A (p.Gly328Glu)
dbSNP
10g.119676540G>CCA378296404BAG3c.986G>C (p.Gly329Ala)
c.809G>C (p.Gly270Ala)
c.983G>C (p.Gly328Ala)
10g.119676540G=CA1940196561BAG3c.986G= (p.Gly329=)
c.809G= (p.Gly270=)
c.983G= (p.Gly328=)
10g.119676540G>TCA378296405BAG3c.986G>T (p.Gly329Val)
c.809G>T (p.Gly270Val)
c.983G>T (p.Gly328Val)
10g.119676541A>CCA471634821BAG3c.987A>C (p.Gly329=)
c.810A>C (p.Gly270=)
c.984A>C (p.Gly328=)
10g.119676541A>GCA471634819BAG3c.987A>G (p.Gly329=)
c.810A>G (p.Gly270=)
c.984A>G (p.Gly328=)
10g.119676541A>TCA471634820BAG3c.987A>T (p.Gly329=)
c.810A>T (p.Gly270=)
c.984A>T (p.Gly328=)
10g.119676542C>ACA378296406BAG3c.988C>A (p.Pro330Thr)
c.811C>A (p.Pro271Thr)
c.985C>A (p.Pro329Thr)
10g.119676542C=CA1940196562BAG3c.988C= (p.Pro330=)
c.811C= (p.Pro271=)
c.985C= (p.Pro329=)
10g.119676542C>GCA378296407BAG3c.988C>G (p.Pro330Ala)
c.811C>G (p.Pro271Ala)
c.985C>G (p.Pro329Ala)
10g.119676542C>TCA5716460BAG3c.988C>T (p.Pro330Ser)
c.811C>T (p.Pro271Ser)
c.985C>T (p.Pro329Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676543C>ACA378296408BAG3c.989C>A (p.Pro330Gln)
c.812C>A (p.Pro271Gln)
c.986C>A (p.Pro329Gln)
10g.119676543C=CA1940196563BAG3c.989C= (p.Pro330=)
c.812C= (p.Pro271=)
c.986C= (p.Pro329=)
10g.119676543C>GCA378296409BAG3c.989C>G (p.Pro330Arg)
c.812C>G (p.Pro271Arg)
c.986C>G (p.Pro329Arg)
10g.119676543C>TCA378296410BAG3c.989C>T (p.Pro330Leu)
c.812C>T (p.Pro271Leu)
c.986C>T (p.Pro329Leu)
ClinVar dbSNP gnomAD v4
10g.119676544A=CA1940196564BAG3c.990A= (p.Pro330=)
c.813A= (p.Pro271=)
c.987A= (p.Pro329=)
10g.119676544A>CCA471634822BAG3c.990A>C (p.Pro330=)
c.813A>C (p.Pro271=)
c.987A>C (p.Pro329=)
10g.119676544A>GCA471634823BAG3c.990A>G (p.Pro330=)
c.813A>G (p.Pro271=)
c.987A>G (p.Pro329=)
dbSNP gnomAD v3 gnomAD v4
10g.119676544A>TCA471634824BAG3c.990A>T (p.Pro330=)
c.813A>T (p.Pro271=)
c.987A>T (p.Pro329=)
10g.119676545G>ACA378296413BAG3c.991G>A (p.Glu331Lys)
c.814G>A (p.Glu272Lys)
c.988G>A (p.Glu330Lys)
10g.119676545G>CCA378296411BAG3c.991G>C (p.Glu331Gln)
c.814G>C (p.Glu272Gln)
c.988G>C (p.Glu330Gln)
10g.119676545G>TCA378296412BAG3c.991G>T (p.Glu331Ter)
c.814G>T (p.Glu272Ter)
c.988G>T (p.Glu330Ter)
10g.119676546A>CCA378296414BAG3c.992A>C (p.Glu331Ala)
c.815A>C (p.Glu272Ala)
c.989A>C (p.Glu330Ala)
10g.119676546A>GCA378296415BAG3c.992A>G (p.Glu331Gly)
c.815A>G (p.Glu272Gly)
c.989A>G (p.Glu330Gly)
10g.119676546A>TCA378296416BAG3c.992A>T (p.Glu331Val)
c.815A>T (p.Glu272Val)
c.989A>T (p.Glu330Val)
10g.119676547A>CCA378296417BAG3c.993A>C (p.Glu331Asp)
c.816A>C (p.Glu272Asp)
c.990A>C (p.Glu330Asp)
10g.119676547A>GCA471634825BAG3c.993A>G (p.Glu331=)
c.816A>G (p.Glu272=)
c.990A>G (p.Glu330=)
10g.119676547A>TCA378296418BAG3c.993A>T (p.Glu331Asp)
c.816A>T (p.Glu272Asp)
c.990A>T (p.Glu330Asp)
10g.119676548C>ACA5716461BAG3c.994C>A (p.Leu332Ile)
c.817C>A (p.Leu273Ile)
c.991C>A (p.Leu331Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676548C=CA1940196565BAG3c.994C= (p.Leu332=)
c.817C= (p.Leu273=)
c.991C= (p.Leu331=)
10g.119676548C>GCA378296419BAG3c.994C>G (p.Leu332Val)
c.817C>G (p.Leu273Val)
c.991C>G (p.Leu331Val)
10g.119676548C>TCA378296420BAG3c.994C>T (p.Leu332Phe)
c.817C>T (p.Leu273Phe)
c.991C>T (p.Leu331Phe)
ClinVar
10g.119676549T>ACA378296421BAG3c.995T>A (p.Leu332His)
c.818T>A (p.Leu273His)
c.992T>A (p.Leu331His)
10g.119676549T>CCA378296422BAG3c.995T>C (p.Leu332Pro)
c.818T>C (p.Leu273Pro)
c.992T>C (p.Leu331Pro)
10g.119676549T>GCA378296423BAG3c.995T>G (p.Leu332Arg)
c.818T>G (p.Leu273Arg)
c.992T>G (p.Leu331Arg)
10g.119676553_119676567delCA2611160293BAG3c.999_1013del (p.Pro334_Pro338del)
c.822_836del (p.Pro275_Pro279del)
c.996_1010del (p.Pro333_Pro337del)
gnomAD v4
10g.119676550C>ACA471634826BAG3c.996C>A (p.Leu332=)
c.819C>A (p.Leu273=)
c.993C>A (p.Leu331=)
10g.119676550C>GCA471634827BAG3c.996C>G (p.Leu332=)
c.819C>G (p.Leu273=)
c.993C>G (p.Leu331=)
ClinVar dbSNP
10g.119676550C>TCA471634828BAG3c.996C>T (p.Leu332=)
c.819C>T (p.Leu273=)
c.993C>T (p.Leu331=)
ClinVar gnomAD v4
10g.119676551C>ACA378296424BAG3c.997C>A (p.Pro333Thr)
c.820C>A (p.Pro274Thr)
c.994C>A (p.Pro332Thr)
10g.119676551C=CA1940196566BAG3c.997C= (p.Pro333=)
c.820C= (p.Pro274=)
c.994C= (p.Pro332=)
10g.119676551C>GCA378296425BAG3c.997C>G (p.Pro333Ala)
c.820C>G (p.Pro274Ala)
c.994C>G (p.Pro332Ala)
10g.119676551C>TCA378296426BAG3c.997C>T (p.Pro333Ser)
c.820C>T (p.Pro274Ser)
c.994C>T (p.Pro332Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676552C>ACA378296427BAG3c.998C>A (p.Pro333His)
c.821C>A (p.Pro274His)
c.995C>A (p.Pro332His)
10g.119676552C>GCA378296428BAG3c.998C>G (p.Pro333Arg)
c.821C>G (p.Pro274Arg)
c.995C>G (p.Pro332Arg)
10g.119676552C>TCA378296429BAG3c.998C>T (p.Pro333Leu)
c.821C>T (p.Pro274Leu)
c.995C>T (p.Pro332Leu)
ClinVar
10g.119676553T>ACA471634829BAG3c.999T>A (p.Pro333=)
c.822T>A (p.Pro274=)
c.996T>A (p.Pro332=)
ClinVar dbSNP gnomAD v4
10g.119676553T>CCA471634830BAG3c.999T>C (p.Pro333=)
c.822T>C (p.Pro274=)
c.996T>C (p.Pro332=)
10g.119676553T>GCA471634831BAG3c.999T>G (p.Pro333=)
c.822T>G (p.Pro274=)
c.996T>G (p.Pro332=)
10g.119676554C>ACA378296430BAG3c.1000C>A (p.Pro334Thr)
c.823C>A (p.Pro275Thr)
c.997C>A (p.Pro333Thr)
10g.119676554C>GCA378296431BAG3c.1000C>G (p.Pro334Ala)
c.823C>G (p.Pro275Ala)
c.997C>G (p.Pro333Ala)
10g.119676554C>TCA378296432BAG3c.1000C>T (p.Pro334Ser)
c.823C>T (p.Pro275Ser)
c.997C>T (p.Pro333Ser)
gnomAD v4
10g.119676555C>ACA378296435BAG3c.1001C>A (p.Pro334His)
c.824C>A (p.Pro275His)
c.998C>A (p.Pro333His)
10g.119676555C=CA1940196567BAG3c.1001C= (p.Pro334=)
c.824C= (p.Pro275=)
c.998C= (p.Pro333=)
10g.119676555C>GCA378296433BAG3c.1001C>G (p.Pro334Arg)
c.824C>G (p.Pro275Arg)
c.998C>G (p.Pro333Arg)
10g.119676555C>TCA378296434BAG3c.1001C>T (p.Pro334Leu)
c.824C>T (p.Pro275Leu)
c.998C>T (p.Pro333Leu)
dbSNP gnomAD v4
10g.119676556T>ACA471634832BAG3c.1002T>A (p.Pro334=)
c.825T>A (p.Pro275=)
c.999T>A (p.Pro333=)
gnomAD v4
10g.119676556T>CCA471634833BAG3c.1002T>C (p.Pro334=)
c.825T>C (p.Pro275=)
c.999T>C (p.Pro333=)
10g.119676556T>GCA282452BAG3c.1002T>G (p.Pro334=)
c.825T>G (p.Pro275=)
c.999T>G (p.Pro333=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676556T=CA1940196568BAG3c.1002T= (p.Pro334=)
c.825T= (p.Pro275=)
c.999T= (p.Pro333=)
10g.119676557G>ACA378296438BAG3c.1003G>A (p.Gly335Arg)
c.826G>A (p.Gly276Arg)
c.1000G>A (p.Gly334Arg)
10g.119676557G>CCA378296436BAG3c.1003G>C (p.Gly335Arg)
c.826G>C (p.Gly276Arg)
c.1000G>C (p.Gly334Arg)
10g.119676557G>TCA378296437BAG3c.1003G>T (p.Gly335Ter)
c.826G>T (p.Gly276Ter)
c.1000G>T (p.Gly334Ter)
10g.119676558G>ACA378296439BAG3c.1004G>A (p.Gly335Glu)
c.827G>A (p.Gly276Glu)
c.1001G>A (p.Gly334Glu)
10g.119676558G>CCA378296440BAG3c.1004G>C (p.Gly335Ala)
c.827G>C (p.Gly276Ala)
c.1001G>C (p.Gly334Ala)
10g.119676558G>TCA378296441BAG3c.1004G>T (p.Gly335Val)
c.827G>T (p.Gly276Val)
c.1001G>T (p.Gly334Val)
10g.119676559A>CCA471634834BAG3c.1005A>C (p.Gly335=)
c.828A>C (p.Gly276=)
c.1002A>C (p.Gly334=)
10g.119676559A>GCA471634835BAG3c.1005A>G (p.Gly335=)
c.828A>G (p.Gly276=)
c.1002A>G (p.Gly334=)
gnomAD v4
10g.119676559A>TCA471634836BAG3c.1005A>T (p.Gly335=)
c.828A>T (p.Gly276=)
c.1002A>T (p.Gly334=)
10g.119676560C>ACA378296442BAG3c.1006C>A (p.His336Asn)
c.829C>A (p.His277Asn)
c.1003C>A (p.His335Asn)
10g.119676560C>GCA378296443BAG3c.1006C>G (p.His336Asp)
c.829C>G (p.His277Asp)
c.1003C>G (p.His335Asp)
10g.119676560C>TCA378296444BAG3c.1006C>T (p.His336Tyr)
c.829C>T (p.His277Tyr)
c.1003C>T (p.His335Tyr)
10g.119676561A>CCA378296445BAG3c.1007A>C (p.His336Pro)
c.830A>C (p.His277Pro)
c.1004A>C (p.His335Pro)
gnomAD v4
10g.119676561A>GCA378296446BAG3c.1007A>G (p.His336Arg)
c.830A>G (p.His277Arg)
c.1004A>G (p.His335Arg)
10g.119676561A>TCA378296447BAG3c.1007A>T (p.His336Leu)
c.830A>T (p.His277Leu)
c.1004A>T (p.His335Leu)
10g.119676562C>ACA378296448BAG3c.1008C>A (p.His336Gln)
c.831C>A (p.His277Gln)
c.1005C>A (p.His335Gln)
10g.119676562C>GCA378296449BAG3c.1008C>G (p.His336Gln)
c.831C>G (p.His277Gln)
c.1005C>G (p.His335Gln)
10g.119676562C>TCA471634837BAG3c.1008C>T (p.His336=)
c.831C>T (p.His277=)
c.1005C>T (p.His335=)
10g.119676563A>CCA378296450BAG3c.1009A>C (p.Ile337Leu)
c.832A>C (p.Ile278Leu)
c.1006A>C (p.Ile336Leu)
10g.119676563A>GCA378296452BAG3c.1009A>G (p.Ile337Val)
c.832A>G (p.Ile278Val)
c.1006A>G (p.Ile336Val)
dbSNP gnomAD v4
10g.119676563A>TCA378296451BAG3c.1009A>T (p.Ile337Phe)
c.832A>T (p.Ile278Phe)
c.1006A>T (p.Ile336Phe)
10g.119676563dupCA2740093564BAG3c.1009dup (p.Ile337AsnfsTer13)
c.832dup (p.Ile278AsnfsTer13)
c.1006dup (p.Ile336AsnfsTer13)
ClinVar
10g.119676564T>ACA378296453BAG3c.1010T>A (p.Ile337Asn)
c.833T>A (p.Ile278Asn)
c.1007T>A (p.Ile336Asn)
dbSNP gnomAD v2 gnomAD v4
10g.119676564T>CCA378296454BAG3c.1010T>C (p.Ile337Thr)
c.833T>C (p.Ile278Thr)
c.1007T>C (p.Ile336Thr)
10g.119676564T>GCA378296455BAG3c.1010T>G (p.Ile337Ser)
c.833T>G (p.Ile278Ser)
c.1007T>G (p.Ile336Ser)
10g.119676564T=CA1940196569BAG3c.1010T= (p.Ile337=)
c.833T= (p.Ile278=)
c.1007T= (p.Ile336=)
10g.119676565C>ACA471634838BAG3c.1011C>A (p.Ile337=)
c.834C>A (p.Ile278=)
c.1008C>A (p.Ile336=)
ClinVar dbSNP gnomAD v4
10g.119676565C=CA1940196570BAG3c.1011C= (p.Ile337=)
c.834C= (p.Ile278=)
c.1008C= (p.Ile336=)
10g.119676565C>GCA378296456BAG3c.1011C>G (p.Ile337Met)
c.834C>G (p.Ile278Met)
c.1008C>G (p.Ile336Met)
10g.119676565C>TCA471634839BAG3c.1011C>T (p.Ile337=)
c.834C>T (p.Ile278=)
c.1008C>T (p.Ile336=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676567dupCA2580082415BAG3c.1013dup (p.Ile339AsnfsTer11)
c.836dup (p.Ile280AsnfsTer11)
c.1010dup (p.Ile338AsnfsTer11)
ClinVar
10g.119676566C>ACA378296457BAG3c.1012C>A (p.Pro338Thr)
c.835C>A (p.Pro279Thr)
c.1009C>A (p.Pro337Thr)
10g.119676566C=CA1940196571BAG3c.1012C= (p.Pro338=)
c.835C= (p.Pro279=)
c.1009C= (p.Pro337=)
10g.119676566C>GCA378296458BAG3c.1012C>G (p.Pro338Ala)
c.835C>G (p.Pro279Ala)
c.1009C>G (p.Pro337Ala)
10g.119676566C>TCA378296459BAG3c.1012C>T (p.Pro338Ser)
c.835C>T (p.Pro279Ser)
c.1009C>T (p.Pro337Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676567C>ACA378296460BAG3c.1013C>A (p.Pro338Gln)
c.836C>A (p.Pro279Gln)
c.1010C>A (p.Pro337Gln)
10g.119676567C=CA1940196572BAG3c.1013C= (p.Pro338=)
c.836C= (p.Pro279=)
c.1010C= (p.Pro337=)
10g.119676567C>GCA378296461BAG3c.1013C>G (p.Pro338Arg)
c.836C>G (p.Pro279Arg)
c.1010C>G (p.Pro337Arg)
10g.119676567C>TCA378296462BAG3c.1013C>T (p.Pro338Leu)
c.836C>T (p.Pro279Leu)
c.1010C>T (p.Pro337Leu)
dbSNP gnomAD v4
10g.119676568A>CCA471634840BAG3c.1014A>C (p.Pro338=)
c.837A>C (p.Pro279=)
c.1011A>C (p.Pro337=)
10g.119676568A>GCA471634842BAG3c.1014A>G (p.Pro338=)
c.837A>G (p.Pro279=)
c.1011A>G (p.Pro337=)
10g.119676568A>TCA471634841BAG3c.1014A>T (p.Pro338=)
c.837A>T (p.Pro279=)
c.1011A>T (p.Pro337=)
10g.119676569A=CA1940196573BAG3c.1015A= (p.Ile339=)
c.838A= (p.Ile280=)
c.1012A= (p.Ile338=)
10g.119676569A>CCA378296464BAG3c.1015A>C (p.Ile339Leu)
c.838A>C (p.Ile280Leu)
c.1012A>C (p.Ile338Leu)
10g.119676569A>GCA5716462BAG3c.1015A>G (p.Ile339Val)
c.838A>G (p.Ile280Val)
c.1012A>G (p.Ile338Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676569A>TCA378296463BAG3c.1015A>T (p.Ile339Phe)
c.838A>T (p.Ile280Phe)
c.1012A>T (p.Ile338Phe)
dbSNP gnomAD v2 gnomAD v4
10g.119676570T>ACA378296467BAG3c.1016T>A (p.Ile339Asn)
c.839T>A (p.Ile280Asn)
c.1013T>A (p.Ile338Asn)
10g.119676570T>CCA378296465BAG3c.1016T>C (p.Ile339Thr)
c.839T>C (p.Ile280Thr)
c.1013T>C (p.Ile338Thr)
10g.119676570T>GCA378296466BAG3c.1016T>G (p.Ile339Ser)
c.839T>G (p.Ile280Ser)
c.1013T>G (p.Ile338Ser)
10g.119676571T>ACA471634843BAG3c.1017T>A (p.Ile339=)
c.840T>A (p.Ile280=)
c.1014T>A (p.Ile338=)
ClinVar dbSNP
10g.119676571T>CCA471634844BAG3c.1017T>C (p.Ile339=)
c.840T>C (p.Ile280=)
c.1014T>C (p.Ile338=)
10g.119676571T>GCA378296468BAG3c.1017T>G (p.Ile339Met)
c.840T>G (p.Ile280Met)
c.1014T>G (p.Ile338Met)
10g.119676572C>ACA378296469BAG3c.1018C>A (p.Gln340Lys)
c.841C>A (p.Gln281Lys)
c.1015C>A (p.Gln339Lys)
10g.119676572C>GCA378296470BAG3c.1018C>G (p.Gln340Glu)
c.841C>G (p.Gln281Glu)
c.1015C>G (p.Gln339Glu)
10g.119676572C>TCA378296471BAG3c.1018C>T (p.Gln340Ter)
c.841C>T (p.Gln281Ter)
c.1015C>T (p.Gln339Ter)
dbSNP
10g.119676573A>CCA378296472BAG3c.1019A>C (p.Gln340Pro)
c.842A>C (p.Gln281Pro)
c.1016A>C (p.Gln339Pro)
10g.119676573A>GCA378296473BAG3c.1019A>G (p.Gln340Arg)
c.842A>G (p.Gln281Arg)
c.1016A>G (p.Gln339Arg)
10g.119676573A>TCA378296474BAG3c.1019A>T (p.Gln340Leu)
c.842A>T (p.Gln281Leu)
c.1016A>T (p.Gln339Leu)
10g.119676574A=CA1940196574BAG3c.1020A= (p.Gln340=)
c.843A= (p.Gln281=)
c.1017A= (p.Gln339=)
10g.119676574A>CCA378296475BAG3c.1020A>C (p.Gln340His)
c.843A>C (p.Gln281His)
c.1017A>C (p.Gln339His)
10g.119676574A>GCA5716463BAG3c.1020A>G (p.Gln340=)
c.843A>G (p.Gln281=)
c.1017A>G (p.Gln339=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676574A>TCA378296476BAG3c.1020A>T (p.Gln340His)
c.843A>T (p.Gln281His)
c.1017A>T (p.Gln339His)
10g.119676575G>ACA378296479BAG3c.1021G>A (p.Val341Met)
c.844G>A (p.Val282Met)
c.1018G>A (p.Val340Met)
gnomAD v4
10g.119676575G>CCA378296478BAG3c.1021G>C (p.Val341Leu)
c.844G>C (p.Val282Leu)
c.1018G>C (p.Val340Leu)
10g.119676575G>TCA378296477BAG3c.1021G>T (p.Val341Leu)
c.844G>T (p.Val282Leu)
c.1018G>T (p.Val340Leu)
10g.119676576T>ACA378296480BAG3c.1022T>A (p.Val341Glu)
c.845T>A (p.Val282Glu)
c.1019T>A (p.Val340Glu)
10g.119676576T>CCA378296481BAG3c.1022T>C (p.Val341Ala)
c.845T>C (p.Val282Ala)
c.1019T>C (p.Val340Ala)
10g.119676576T>GCA378296482BAG3c.1022T>G (p.Val341Gly)
c.845T>G (p.Val282Gly)
c.1019T>G (p.Val340Gly)
gnomAD v4
10g.119676577G>ACA471634845BAG3c.1023G>A (p.Val341=)
c.846G>A (p.Val282=)
c.1020G>A (p.Val340=)
ClinVar
10g.119676577G>CCA471634846BAG3c.1023G>C (p.Val341=)
c.846G>C (p.Val282=)
c.1020G>C (p.Val340=)
10g.119676577G>TCA471634847BAG3c.1023G>T (p.Val341=)
c.846G>T (p.Val282=)
c.1020G>T (p.Val340=)
10g.119676578A>CCA378296483BAG3c.1024A>C (p.Ile342Leu)
c.847A>C (p.Ile283Leu)
c.1021A>C (p.Ile341Leu)
gnomAD v4
10g.119676578A>GCA378296484BAG3c.1024A>G (p.Ile342Val)
c.847A>G (p.Ile283Val)
c.1021A>G (p.Ile341Val)
10g.119676578A>TCA378296485BAG3c.1024A>T (p.Ile342Phe)
c.847A>T (p.Ile283Phe)
c.1021A>T (p.Ile341Phe)
10g.119676579T>ACA378296486BAG3c.1025T>A (p.Ile342Asn)
c.848T>A (p.Ile283Asn)
c.1022T>A (p.Ile341Asn)
10g.119676579T>CCA5716464BAG3c.1025T>C (p.Ile342Thr)
c.848T>C (p.Ile283Thr)
c.1022T>C (p.Ile341Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676579T>GCA378296487BAG3c.1025T>G (p.Ile342Ser)
c.848T>G (p.Ile283Ser)
c.1022T>G (p.Ile341Ser)
10g.119676579T=CA1940196575BAG3c.1025T= (p.Ile342=)
c.848T= (p.Ile283=)
c.1022T= (p.Ile341=)
10g.119676580C>ACA471634848BAG3c.1026C>A (p.Ile342=)
c.849C>A (p.Ile283=)
c.1023C>A (p.Ile341=)
10g.119676580C>GCA378296488BAG3c.1026C>G (p.Ile342Met)
c.849C>G (p.Ile283Met)
c.1023C>G (p.Ile341Met)
ClinVar
10g.119676580C>TCA471634849BAG3c.1026C>T (p.Ile342=)
c.849C>T (p.Ile283=)
c.1023C>T (p.Ile341=)
10g.119676581delCA1139532244BAG3c.1027del (p.Arg343AlafsTer20)
c.850del (p.Arg284AlafsTer20)
c.1024del (p.Arg342AlafsTer20)
dbSNP
10g.119676581C>ACA378296489BAG3c.1027C>A (p.Arg343Ser)
c.850C>A (p.Arg284Ser)
c.1024C>A (p.Arg342Ser)
10g.119676581C=CA1940196576BAG3c.1027C= (p.Arg343=)
c.850C= (p.Arg284=)
c.1024C= (p.Arg342=)
10g.119676581C>GCA378296490BAG3c.1027C>G (p.Arg343Gly)
c.850C>G (p.Arg284Gly)
c.1024C>G (p.Arg342Gly)
10g.119676581C>TCA5716465BAG3c.1027C>T (p.Arg343Cys)
c.850C>T (p.Arg284Cys)
c.1024C>T (p.Arg342Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676582G>ACA5716466BAG3c.1028G>A (p.Arg343His)
c.851G>A (p.Arg284His)
c.1025G>A (p.Arg342His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676582G>CCA378296491BAG3c.1028G>C (p.Arg343Pro)
c.851G>C (p.Arg284Pro)
c.1025G>C (p.Arg342Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676582G=CA1940196577BAG3c.1028G= (p.Arg343=)
c.851G= (p.Arg284=)
c.1025G= (p.Arg342=)
10g.119676582G>TCA5716467BAG3c.1028G>T (p.Arg343Leu)
c.851G>T (p.Arg284Leu)
c.1025G>T (p.Arg342Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676583C>ACA5716468BAG3c.1029C>A (p.Arg343=)
c.852C>A (p.Arg284=)
c.1026C>A (p.Arg342=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676583C=CA1940196578BAG3c.1029C= (p.Arg343=)
c.852C= (p.Arg284=)
c.1026C= (p.Arg342=)
10g.119676583C>GCA471634850BAG3c.1029C>G (p.Arg343=)
c.852C>G (p.Arg284=)
c.1026C>G (p.Arg342=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676583C>TCA5716469BAG3c.1029C>T (p.Arg343=)
c.852C>T (p.Arg284=)
c.1026C>T (p.Arg342=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676583_119676585delinsCAACA1940196579BAG3c.1029_1031delinsCAA (p.Arg343=)
c.852_854delinsCAA (p.Arg284=)
c.1026_1028delinsCAA (p.Arg342=)
10g.119676584A>CCA378296492BAG3c.1030A>C (p.Lys344Gln)
c.853A>C (p.Lys285Gln)
c.1027A>C (p.Lys343Gln)
10g.119676584A>GCA378296494BAG3c.1030A>G (p.Lys344Glu)
c.853A>G (p.Lys285Glu)
c.1027A>G (p.Lys343Glu)
10g.119676584A>TCA378296493BAG3c.1030A>T (p.Lys344Ter)
c.853A>T (p.Lys285Ter)
c.1027A>T (p.Lys343Ter)
10g.119676585_119676586delCA1139661707BAG3c.1031_1032del (p.Lys344ArgfsTer5)
c.854_855del (p.Lys285ArgfsTer5)
c.1028_1029del (p.Lys343ArgfsTer5)
ClinVar dbSNP
10g.119676585A>CCA378296495BAG3c.1031A>C (p.Lys344Thr)
c.854A>C (p.Lys285Thr)
c.1028A>C (p.Lys343Thr)
10g.119676585A>GCA378296496BAG3c.1031A>G (p.Lys344Arg)
c.854A>G (p.Lys285Arg)
c.1028A>G (p.Lys343Arg)
gnomAD v4
10g.119676585A>TCA378296497BAG3c.1031A>T (p.Lys344Ile)
c.854A>T (p.Lys285Ile)
c.1028A>T (p.Lys343Ile)
10g.119676586A>CCA378296498BAG3c.1032A>C (p.Lys344Asn)
c.855A>C (p.Lys285Asn)
c.1029A>C (p.Lys343Asn)
10g.119676586A>GCA471634852BAG3c.1032A>G (p.Lys344=)
c.855A>G (p.Lys285=)
c.1029A>G (p.Lys343=)
10g.119676586A>TCA378296499BAG3c.1032A>T (p.Lys344Asn)
c.855A>T (p.Lys285Asn)
c.1029A>T (p.Lys343Asn)
ClinVar dbSNP
10g.119676586_119676591delinsAGAGGTCA1940196580BAG3c.1032_1037delinsAGAGGT (p.Lys344=)
c.855_860delinsAGAGGT (p.Lys285=)
c.1029_1034delinsAGAGGT (p.Lys343=)
10g.119676587G>ACA378296500BAG3c.1033G>A (p.Glu345Lys)
c.856G>A (p.Glu286Lys)
c.1030G>A (p.Glu344Lys)
10g.119676587G>CCA378296501BAG3c.1033G>C (p.Glu345Gln)
c.856G>C (p.Glu286Gln)
c.1030G>C (p.Glu344Gln)
10g.119676587G>TCA378296502BAG3c.1033G>T (p.Glu345Ter)
c.856G>T (p.Glu286Ter)
c.1030G>T (p.Glu344Ter)
COSMIC
10g.119676588_119676592delCA658797543BAG3c.1034_1038del (p.Glu345GlyfsTer3)
c.857_861del (p.Glu286GlyfsTer3)
c.1031_1035del (p.Glu344GlyfsTer3)
ClinVar dbSNP
10g.119676588A=CA1940196581BAG3c.1034A= (p.Glu345=)
c.857A= (p.Glu286=)
c.1031A= (p.Glu344=)
10g.119676588A>CCA378296503BAG3c.1034A>C (p.Glu345Ala)
c.857A>C (p.Glu286Ala)
c.1031A>C (p.Glu344Ala)
10g.119676588A>GCA378296504BAG3c.1034A>G (p.Glu345Gly)
c.857A>G (p.Glu286Gly)
c.1031A>G (p.Glu344Gly)
10g.119676588A>TCA5716470BAG3c.1034A>T (p.Glu345Val)
c.857A>T (p.Glu286Val)
c.1031A>T (p.Glu344Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676589G>ACA471634853BAG3c.1035G>A (p.Glu345=)
c.858G>A (p.Glu286=)
c.1032G>A (p.Glu344=)
ClinVar dbSNP gnomAD v4
10g.119676589G>CCA16605822BAG3c.1035G>C (p.Glu345Asp)
c.858G>C (p.Glu286Asp)
c.1032G>C (p.Glu344Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676589G=CA1940196582BAG3c.1035G= (p.Glu345=)
c.858G= (p.Glu286=)
c.1032G= (p.Glu344=)
10g.119676589G>TCA378296505BAG3c.1035G>T (p.Glu345Asp)
c.858G>T (p.Glu286Asp)
c.1032G>T (p.Glu344Asp)
10g.119676590G>ACA378296506BAG3c.1036G>A (p.Val346Met)
c.859G>A (p.Val287Met)
c.1033G>A (p.Val345Met)
10g.119676590G>CCA378296507BAG3c.1036G>C (p.Val346Leu)
c.859G>C (p.Val287Leu)
c.1033G>C (p.Val345Leu)
10g.119676590G>TCA378296508BAG3c.1036G>T (p.Val346Leu)
c.859G>T (p.Val287Leu)
c.1033G>T (p.Val345Leu)
10g.119676591T>ACA378296509BAG3c.1037T>A (p.Val346Glu)
c.860T>A (p.Val287Glu)
c.1034T>A (p.Val345Glu)
10g.119676591T>CCA378296510BAG3c.1037T>C (p.Val346Ala)
c.860T>C (p.Val287Ala)
c.1034T>C (p.Val345Ala)
10g.119676591T>GCA378296511BAG3c.1037T>G (p.Val346Gly)
c.860T>G (p.Val287Gly)
c.1034T>G (p.Val345Gly)
10g.119676592G>ACA471634854BAG3c.1038G>A (p.Val346=)
c.861G>A (p.Val287=)
c.1035G>A (p.Val345=)
gnomAD v4
10g.119676592G>CCA471634855BAG3c.1038G>C (p.Val346=)
c.861G>C (p.Val287=)
c.1035G>C (p.Val345=)
10g.119676592G=CA1940196583BAG3c.1038G= (p.Val346=)
c.861G= (p.Val287=)
c.1035G= (p.Val345=)
10g.119676592G>TCA214224780BAG3c.1038G>T (p.Val346=)
c.861G>T (p.Val287=)
c.1035G>T (p.Val345=)
dbSNP gnomAD v4
10g.119676593G>ACA378296512BAG3c.1039G>A (p.Asp347Asn)
c.862G>A (p.Asp288Asn)
c.1036G>A (p.Asp346Asn)
10g.119676593G>CCA214224786BAG3c.1039G>C (p.Asp347His)
c.862G>C (p.Asp288His)
c.1036G>C (p.Asp346His)
dbSNP gnomAD v4
10g.119676593G=CA1940196584BAG3c.1039G= (p.Asp347=)
c.862G= (p.Asp288=)
c.1036G= (p.Asp346=)
10g.119676593G>TCA378296513BAG3c.1039G>T (p.Asp347Tyr)
c.862G>T (p.Asp288Tyr)
c.1036G>T (p.Asp346Tyr)
10g.119676594A=CA1940196585BAG3c.1040A= (p.Asp347=)
c.863A= (p.Asp288=)
c.1037A= (p.Asp346=)
10g.119676594A>CCA378296514BAG3c.1040A>C (p.Asp347Ala)
c.863A>C (p.Asp288Ala)
c.1037A>C (p.Asp346Ala)
gnomAD v4
10g.119676594A>GCA378296515BAG3c.1040A>G (p.Asp347Gly)
c.863A>G (p.Asp288Gly)
c.1037A>G (p.Asp346Gly)
gnomAD v4
10g.119676594A>TCA5716471BAG3c.1040A>T (p.Asp347Val)
c.863A>T (p.Asp288Val)
c.1037A>T (p.Asp346Val)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676595T>ACA378296517BAG3c.1041T>A (p.Asp347Glu)
c.864T>A (p.Asp288Glu)
c.1038T>A (p.Asp346Glu)
10g.119676595T>CCA471634859BAG3c.1041T>C (p.Asp347=)
c.864T>C (p.Asp288=)
c.1038T>C (p.Asp346=)
10g.119676595T>GCA378296516BAG3c.1041T>G (p.Asp347Glu)
c.864T>G (p.Asp288Glu)
c.1038T>G (p.Asp346Glu)
10g.119676596T>ACA378296518BAG3c.1042T>A (p.Ser348Thr)
c.865T>A (p.Ser289Thr)
c.1039T>A (p.Ser347Thr)
10g.119676596T>CCA378296519BAG3c.1042T>C (p.Ser348Pro)
c.865T>C (p.Ser289Pro)
c.1039T>C (p.Ser347Pro)
10g.119676596T>GCA378296520BAG3c.1042T>G (p.Ser348Ala)
c.865T>G (p.Ser289Ala)
c.1039T>G (p.Ser347Ala)
10g.119676597C>ACA378296521BAG3c.1043C>A (p.Ser348Tyr)
c.866C>A (p.Ser289Tyr)
c.1040C>A (p.Ser347Tyr)
10g.119676597C>GCA378296522BAG3c.1043C>G (p.Ser348Cys)
c.866C>G (p.Ser289Cys)
c.1040C>G (p.Ser347Cys)
10g.119676597C>TCA378296523BAG3c.1043C>T (p.Ser348Phe)
c.866C>T (p.Ser289Phe)
c.1040C>T (p.Ser347Phe)
10g.119676598T>ACA471634863BAG3c.1044T>A (p.Ser348=)
c.867T>A (p.Ser289=)
c.1041T>A (p.Ser347=)
10g.119676598T>CCA471634864BAG3c.1044T>C (p.Ser348=)
c.867T>C (p.Ser289=)
c.1041T>C (p.Ser347=)
gnomAD v4
10g.119676598T>GCA471634865BAG3c.1044T>G (p.Ser348=)
c.867T>G (p.Ser289=)
c.1041T>G (p.Ser347=)
10g.119676599A>CCA378296524BAG3c.1045A>C (p.Lys349Gln)
c.868A>C (p.Lys290Gln)
c.1042A>C (p.Lys348Gln)
10g.119676599A>GCA378296525BAG3c.1045A>G (p.Lys349Glu)
c.868A>G (p.Lys290Glu)
c.1042A>G (p.Lys348Glu)
10g.119676599A>TCA378296526BAG3c.1045A>T (p.Lys349Ter)
c.868A>T (p.Lys290Ter)
c.1042A>T (p.Lys348Ter)
10g.119676600A=CA1940196586BAG3c.1046A= (p.Lys349=)
c.869A= (p.Lys290=)
c.1043A= (p.Lys348=)
10g.119676600A>CCA378296527BAG3c.1046A>C (p.Lys349Thr)
c.869A>C (p.Lys290Thr)
c.1043A>C (p.Lys348Thr)
10g.119676600A>GCA378296528BAG3c.1046A>G (p.Lys349Arg)
c.869A>G (p.Lys290Arg)
c.1043A>G (p.Lys348Arg)
10g.119676600A>TCA378296529BAG3c.1046A>T (p.Lys349Ile)
c.869A>T (p.Lys290Ile)
c.1043A>T (p.Lys348Ile)
dbSNP gnomAD v2 gnomAD v4
10g.119676601A=CA1940196587BAG3c.1047A= (p.Lys349=)
c.870A= (p.Lys290=)
c.1044A= (p.Lys348=)
10g.119676601A>CCA378296531BAG3c.1047A>C (p.Lys349Asn)
c.870A>C (p.Lys290Asn)
c.1044A>C (p.Lys348Asn)
10g.119676601A>GCA5716472BAG3c.1047A>G (p.Lys349=)
c.870A>G (p.Lys290=)
c.1044A>G (p.Lys348=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676601A>TCA378296530BAG3c.1047A>T (p.Lys349Asn)
c.870A>T (p.Lys290Asn)
c.1044A>T (p.Lys348Asn)
ClinVar
10g.119676602C>ACA378296532BAG3c.1048C>A (p.Pro350Thr)
c.871C>A (p.Pro291Thr)
c.1045C>A (p.Pro349Thr)
10g.119676602C>GCA378296533BAG3c.1048C>G (p.Pro350Ala)
c.871C>G (p.Pro291Ala)
c.1045C>G (p.Pro349Ala)
10g.119676602C>TCA378296534BAG3c.1048C>T (p.Pro350Ser)
c.871C>T (p.Pro291Ser)
c.1045C>T (p.Pro349Ser)
gnomAD v4
10g.119676603C>ACA378296535BAG3c.1049C>A (p.Pro350His)
c.872C>A (p.Pro291His)
c.1046C>A (p.Pro349His)
10g.119676603C=CA1940196588BAG3c.1049C= (p.Pro350=)
c.872C= (p.Pro291=)
c.1046C= (p.Pro349=)
10g.119676603C>GCA378296536BAG3c.1049C>G (p.Pro350Arg)
c.872C>G (p.Pro291Arg)
c.1046C>G (p.Pro349Arg)
10g.119676603C>TCA5716473BAG3c.1049C>T (p.Pro350Leu)
c.872C>T (p.Pro291Leu)
c.1046C>T (p.Pro349Leu)
dbSNP ExAC gnomAD v2
10g.119676604T>ACA471634868BAG3c.1050T>A (p.Pro350=)
c.873T>A (p.Pro291=)
c.1047T>A (p.Pro349=)
10g.119676604T>CCA471634870BAG3c.1050T>C (p.Pro350=)
c.873T>C (p.Pro291=)
c.1047T>C (p.Pro349=)
10g.119676604T>GCA5716474BAG3c.1050T>G (p.Pro350=)
c.873T>G (p.Pro291=)
c.1047T>G (p.Pro349=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676604T=CA1940196589BAG3c.1050T= (p.Pro350=)
c.873T= (p.Pro291=)
c.1047T= (p.Pro349=)
10g.119676605G>ACA378296537BAG3c.1051G>A (p.Val351Ile)
c.874G>A (p.Val292Ile)
c.1048G>A (p.Val350Ile)
10g.119676605G>CCA378296538BAG3c.1051G>C (p.Val351Leu)
c.874G>C (p.Val292Leu)
c.1048G>C (p.Val350Leu)
10g.119676605G>TCA378296539BAG3c.1051G>T (p.Val351Phe)
c.874G>T (p.Val292Phe)
c.1048G>T (p.Val350Phe)
10g.119676606T>ACA378296540BAG3c.1052T>A (p.Val351Asp)
c.875T>A (p.Val292Asp)
c.1049T>A (p.Val350Asp)
10g.119676606T>CCA378296541BAG3c.1052T>C (p.Val351Ala)
c.875T>C (p.Val292Ala)
c.1049T>C (p.Val350Ala)
10g.119676606T>GCA378296542BAG3c.1052T>G (p.Val351Gly)
c.875T>G (p.Val292Gly)
c.1049T>G (p.Val350Gly)
10g.119676607T>ACA471634871BAG3c.1053T>A (p.Val351=)
c.876T>A (p.Val292=)
c.1050T>A (p.Val350=)
dbSNP gnomAD v2 gnomAD v4
10g.119676607T>CCA471634873BAG3c.1053T>C (p.Val351=)
c.876T>C (p.Val292=)
c.1050T>C (p.Val350=)
10g.119676607T>GCA471634875BAG3c.1053T>G (p.Val351=)
c.876T>G (p.Val292=)
c.1050T>G (p.Val350=)
10g.119676607T=CA1940196590BAG3c.1053T= (p.Val351=)
c.876T= (p.Val292=)
c.1050T= (p.Val350=)
10g.119676608T>ACA378296545BAG3c.1054T>A (p.Ser352Thr)
c.877T>A (p.Ser293Thr)
c.1051T>A (p.Ser351Thr)
ClinVar
10g.119676608T>CCA378296544BAG3c.1054T>C (p.Ser352Pro)
c.877T>C (p.Ser293Pro)
c.1051T>C (p.Ser351Pro)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676608T>GCA378296543BAG3c.1054T>G (p.Ser352Ala)
c.877T>G (p.Ser293Ala)
c.1051T>G (p.Ser351Ala)
10g.119676608T=CA1940196591BAG3c.1054T= (p.Ser352=)
c.877T= (p.Ser293=)
c.1051T= (p.Ser351=)
10g.119676609C>ACA378296546BAG3c.1055C>A (p.Ser352Tyr)
c.878C>A (p.Ser293Tyr)
c.1052C>A (p.Ser351Tyr)
10g.119676609C=CA1940196592BAG3c.1055C= (p.Ser352=)
c.878C= (p.Ser293=)
c.1052C= (p.Ser351=)
10g.119676609C>GCA378296548BAG3c.1055C>G (p.Ser352Cys)
c.878C>G (p.Ser293Cys)
c.1052C>G (p.Ser351Cys)
ClinVar dbSNP gnomAD v4
10g.119676609C>TCA378296547BAG3c.1055C>T (p.Ser352Phe)
c.878C>T (p.Ser293Phe)
c.1052C>T (p.Ser351Phe)
dbSNP
10g.119676611delCA1139532492BAG3c.1057del (p.Gln353ArgfsTer10)
c.880del (p.Gln294ArgfsTer10)
c.1054del (p.Gln352ArgfsTer10)
ClinVar dbSNP
10g.119676610C>ACA471634878BAG3c.1056C>A (p.Ser352=)
c.879C>A (p.Ser293=)
c.1053C>A (p.Ser351=)
COSMIC
10g.119676610C=CA1940196593BAG3c.1056C= (p.Ser352=)
c.879C= (p.Ser293=)
c.1053C= (p.Ser351=)
10g.119676610C>GCA5716476BAG3c.1056C>G (p.Ser352=)
c.879C>G (p.Ser293=)
c.1053C>G (p.Ser351=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676610C>TCA5716475BAG3c.1056C>T (p.Ser352=)
c.879C>T (p.Ser293=)
c.1053C>T (p.Ser351=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676611C>ACA378296549BAG3c.1057C>A (p.Gln353Lys)
c.880C>A (p.Gln294Lys)
c.1054C>A (p.Gln352Lys)
10g.119676611C=CA1940196594BAG3c.1057C= (p.Gln353=)
c.880C= (p.Gln294=)
c.1054C= (p.Gln352=)
10g.119676611C>GCA378296550BAG3c.1057C>G (p.Gln353Glu)
c.880C>G (p.Gln294Glu)
c.1054C>G (p.Gln352Glu)
10g.119676611C>TCA378296551BAG3c.1057C>T (p.Gln353Ter)
c.880C>T (p.Gln294Ter)
c.1054C>T (p.Gln352Ter)
ClinVar dbSNP
10g.119676612A=CA1940196595BAG3c.1058A= (p.Gln353=)
c.881A= (p.Gln294=)
c.1055A= (p.Gln352=)
10g.119676612A>CCA378296552BAG3c.1058A>C (p.Gln353Pro)
c.881A>C (p.Gln294Pro)
c.1055A>C (p.Gln352Pro)
dbSNP gnomAD v2 gnomAD v4
10g.119676612A>GCA5716477BAG3c.1058A>G (p.Gln353Arg)
c.881A>G (p.Gln294Arg)
c.1055A>G (p.Gln352Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676612A>TCA378296553BAG3c.1058A>T (p.Gln353Leu)
c.881A>T (p.Gln294Leu)
c.1055A>T (p.Gln352Leu)
10g.119676613G>ACA471634882BAG3c.1059G>A (p.Gln353=)
c.882G>A (p.Gln294=)
c.1056G>A (p.Gln352=)
10g.119676613G>CCA378296554BAG3c.1059G>C (p.Gln353His)
c.882G>C (p.Gln294His)
c.1056G>C (p.Gln352His)
10g.119676613G>TCA378296555BAG3c.1059G>T (p.Gln353His)
c.882G>T (p.Gln294His)
c.1056G>T (p.Gln352His)
10g.119676614A=CA1940196596BAG3c.1060A= (p.Lys354=)
c.883A= (p.Lys295=)
c.1057A= (p.Lys353=)
10g.119676614A>CCA378296556BAG3c.1060A>C (p.Lys354Gln)
c.883A>C (p.Lys295Gln)
c.1057A>C (p.Lys353Gln)
10g.119676614A>GCA378296557BAG3c.1060A>G (p.Lys354Glu)
c.883A>G (p.Lys295Glu)
c.1057A>G (p.Lys353Glu)
ClinVar dbSNP
10g.119676614A>TCA378296558BAG3c.1060A>T (p.Lys354Ter)
c.883A>T (p.Lys295Ter)
c.1057A>T (p.Lys353Ter)
10g.119676615A>CCA378296559BAG3c.1061A>C (p.Lys354Thr)
c.884A>C (p.Lys295Thr)
c.1058A>C (p.Lys353Thr)
10g.119676615A>GCA378296561BAG3c.1061A>G (p.Lys354Arg)
c.884A>G (p.Lys295Arg)
c.1058A>G (p.Lys353Arg)
10g.119676615A>TCA378296560BAG3c.1061A>T (p.Lys354Met)
c.884A>T (p.Lys295Met)
c.1058A>T (p.Lys353Met)
10g.119676616G>ACA5716478BAG3c.1062G>A (p.Lys354=)
c.885G>A (p.Lys295=)
c.1059G>A (p.Lys353=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676616G>CCA378296562BAG3c.1062G>C (p.Lys354Asn)
c.885G>C (p.Lys295Asn)
c.1059G>C (p.Lys353Asn)
10g.119676616G=CA1940196597BAG3c.1062G= (p.Lys354=)
c.885G= (p.Lys295=)
c.1059G= (p.Lys353=)
10g.119676616G>TCA378296563BAG3c.1062G>T (p.Lys354Asn)
c.885G>T (p.Lys295Asn)
c.1059G>T (p.Lys353Asn)
10g.119676616_119676617delinsGCCA1940196598BAG3c.1062_1063delinsGC (p.Lys354=)
c.885_886delinsGC (p.Lys295=)
c.1059_1060delinsGC (p.Lys353=)
10g.119676617C>ACA378296564BAG3c.1063C>A (p.Pro355Thr)
c.886C>A (p.Pro296Thr)
c.1060C>A (p.Pro354Thr)
10g.119676617C=CA1940196599BAG3c.1063C= (p.Pro355=)
c.886C= (p.Pro296=)
c.1060C= (p.Pro354=)
10g.119676617C>GCA378296565BAG3c.1063C>G (p.Pro355Ala)
c.886C>G (p.Pro296Ala)
c.1060C>G (p.Pro354Ala)
10g.119676617C>TCA214224856BAG3c.1063C>T (p.Pro355Ser)
c.886C>T (p.Pro296Ser)
c.1060C>T (p.Pro354Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676621dupCA2740093565BAG3c.1067dup (p.Pro357ThrfsTer4)
c.890dup (p.Pro298ThrfsTer4)
c.1064dup (p.Pro356ThrfsTer4)
ClinVar
10g.119676621delCA273654BAG3c.1067del (p.Pro356HisfsTer7)
c.890del (p.Pro297HisfsTer7)
c.1064del (p.Pro355HisfsTer7)
ClinVar dbSNP
10g.119676618C>ACA378296566BAG3c.1064C>A (p.Pro355His)
c.887C>A (p.Pro296His)
c.1061C>A (p.Pro354His)
10g.119676618C=CA1940196600BAG3c.1064C= (p.Pro355=)
c.887C= (p.Pro296=)
c.1061C= (p.Pro354=)
10g.119676618C>GCA378296567BAG3c.1064C>G (p.Pro355Arg)
c.887C>G (p.Pro296Arg)
c.1061C>G (p.Pro354Arg)
10g.119676618C>TCA378296568BAG3c.1064C>T (p.Pro355Leu)
c.887C>T (p.Pro296Leu)
c.1061C>T (p.Pro354Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676619C>ACA471634889BAG3c.1065C>A (p.Pro355=)
c.888C>A (p.Pro296=)
c.1062C>A (p.Pro354=)
10g.119676619C=CA1940196601BAG3c.1065C= (p.Pro355=)
c.888C= (p.Pro296=)
c.1062C= (p.Pro354=)
10g.119676619C>GCA471634890BAG3c.1065C>G (p.Pro355=)
c.888C>G (p.Pro296=)
c.1062C>G (p.Pro354=)
dbSNP gnomAD v4
10g.119676619C>TCA471634891BAG3c.1065C>T (p.Pro355=)
c.888C>T (p.Pro296=)
c.1062C>T (p.Pro354=)
10g.119676620C>ACA378296570BAG3c.1066C>A (p.Pro356Thr)
c.889C>A (p.Pro297Thr)
c.1063C>A (p.Pro355Thr)
10g.119676620C>GCA378296571BAG3c.1066C>G (p.Pro356Ala)
c.889C>G (p.Pro297Ala)
c.1063C>G (p.Pro355Ala)
10g.119676620C>TCA378296569BAG3c.1066C>T (p.Pro356Ser)
c.889C>T (p.Pro297Ser)
c.1063C>T (p.Pro355Ser)
gnomAD v4 COSMIC
10g.119676621C>ACA378296572BAG3c.1067C>A (p.Pro356Gln)
c.890C>A (p.Pro297Gln)
c.1064C>A (p.Pro355Gln)
10g.119676621C>GCA378296573BAG3c.1067C>G (p.Pro356Arg)
c.890C>G (p.Pro297Arg)
c.1064C>G (p.Pro355Arg)
10g.119676621C>TCA378296574BAG3c.1067C>T (p.Pro356Leu)
c.890C>T (p.Pro297Leu)
c.1064C>T (p.Pro355Leu)
10g.119676622A>CCA471634897BAG3c.1068A>C (p.Pro356=)
c.891A>C (p.Pro297=)
c.1065A>C (p.Pro355=)
10g.119676622A>GCA471634898BAG3c.1068A>G (p.Pro356=)
c.891A>G (p.Pro297=)
c.1065A>G (p.Pro355=)
ClinVar dbSNP
10g.119676622A>TCA471634899BAG3c.1068A>T (p.Pro356=)
c.891A>T (p.Pro297=)
c.1065A>T (p.Pro355=)
10g.119676623C>ACA378296575BAG3c.1069C>A (p.Pro357Thr)
c.892C>A (p.Pro298Thr)
c.1066C>A (p.Pro356Thr)
10g.119676623C>GCA378296576BAG3c.1069C>G (p.Pro357Ala)
c.892C>G (p.Pro298Ala)
c.1066C>G (p.Pro356Ala)
10g.119676623C>TCA378296577BAG3c.1069C>T (p.Pro357Ser)
c.892C>T (p.Pro298Ser)
c.1066C>T (p.Pro356Ser)
10g.119676624C>ACA378296578BAG3c.1070C>A (p.Pro357His)
c.893C>A (p.Pro298His)
c.1067C>A (p.Pro356His)
10g.119676624C=CA1940196602BAG3c.1070C= (p.Pro357=)
c.893C= (p.Pro298=)
c.1067C= (p.Pro356=)
10g.119676624C>GCA378296579BAG3c.1070C>G (p.Pro357Arg)
c.893C>G (p.Pro298Arg)
c.1067C>G (p.Pro356Arg)
10g.119676624C>TCA5716479BAG3c.1070C>T (p.Pro357Leu)
c.893C>T (p.Pro298Leu)
c.1067C>T (p.Pro356Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676625T>ACA471634904BAG3c.1071T>A (p.Pro357=)
c.894T>A (p.Pro298=)
c.1068T>A (p.Pro356=)
10g.119676625T>CCA471634906BAG3c.1071T>C (p.Pro357=)
c.894T>C (p.Pro298=)
c.1068T>C (p.Pro356=)
10g.119676625T>GCA471634907BAG3c.1071T>G (p.Pro357=)
c.894T>G (p.Pro298=)
c.1068T>G (p.Pro356=)
10g.119676626C>ACA378296580BAG3c.1072C>A (p.Pro358Thr)
c.895C>A (p.Pro299Thr)
c.1069C>A (p.Pro357Thr)
10g.119676626C=CA1940196603BAG3c.1072C= (p.Pro358=)
c.895C= (p.Pro299=)
c.1069C= (p.Pro357=)
10g.119676626C>GCA378296581BAG3c.1072C>G (p.Pro358Ala)
c.895C>G (p.Pro299Ala)
c.1069C>G (p.Pro357Ala)
10g.119676626C>TCA214224857BAG3c.1072C>T (p.Pro358Ser)
c.895C>T (p.Pro299Ser)
c.1069C>T (p.Pro357Ser)
dbSNP gnomAD v4 COSMIC
10g.119676627C>ACA378296584BAG3c.1073C>A (p.Pro358His)
c.896C>A (p.Pro299His)
c.1070C>A (p.Pro357His)
10g.119676627C=CA1940196604BAG3c.1073C= (p.Pro358=)
c.896C= (p.Pro299=)
c.1070C= (p.Pro357=)
10g.119676627C>GCA378296582BAG3c.1073C>G (p.Pro358Arg)
c.896C>G (p.Pro299Arg)
c.1070C>G (p.Pro357Arg)
10g.119676627C>TCA378296583BAG3c.1073C>T (p.Pro358Leu)
c.896C>T (p.Pro299Leu)
c.1070C>T (p.Pro357Leu)
dbSNP
10g.119676628C>ACA471634910BAG3c.1074C>A (p.Pro358=)
c.897C>A (p.Pro299=)
c.1071C>A (p.Pro357=)
10g.119676628C=CA1940196605BAG3c.1074C= (p.Pro358=)
c.897C= (p.Pro299=)
c.1071C= (p.Pro357=)
10g.119676628C>GCA471634911BAG3c.1074C>G (p.Pro358=)
c.897C>G (p.Pro299=)
c.1071C>G (p.Pro357=)
ClinVar gnomAD v4
10g.119676628C>TCA214224861BAG3c.1074C>T (p.Pro358=)
c.897C>T (p.Pro299=)
c.1071C>T (p.Pro357=)
dbSNP
10g.119676629T>ACA378296585BAG3c.1075T>A (p.Ser359Thr)
c.898T>A (p.Ser300Thr)
c.1072T>A (p.Ser358Thr)
10g.119676629T>CCA5716480BAG3c.1075T>C (p.Ser359Pro)
c.898T>C (p.Ser300Pro)
c.1072T>C (p.Ser358Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676629T>GCA378296586BAG3c.1075T>G (p.Ser359Ala)
c.898T>G (p.Ser300Ala)
c.1072T>G (p.Ser358Ala)
10g.119676629T=CA1940196606BAG3c.1075T= (p.Ser359=)
c.898T= (p.Ser300=)
c.1072T= (p.Ser358=)
10g.119676630C>ACA378296587BAG3c.1076C>A (p.Ser359Tyr)
c.899C>A (p.Ser300Tyr)
c.1073C>A (p.Ser358Tyr)
10g.119676630C>GCA378296588BAG3c.1076C>G (p.Ser359Cys)
c.899C>G (p.Ser300Cys)
c.1073C>G (p.Ser358Cys)
10g.119676630C>TCA378296589BAG3c.1076C>T (p.Ser359Phe)
c.899C>T (p.Ser300Phe)
c.1073C>T (p.Ser358Phe)
gnomAD v4
10g.119676631T>ACA471634912BAG3c.1077T>A (p.Ser359=)
c.900T>A (p.Ser300=)
c.1074T>A (p.Ser358=)
10g.119676631T>CCA471634916BAG3c.1077T>C (p.Ser359=)
c.900T>C (p.Ser300=)
c.1074T>C (p.Ser358=)
10g.119676631T>GCA471634914BAG3c.1077T>G (p.Ser359=)
c.900T>G (p.Ser300=)
c.1074T>G (p.Ser358=)
10g.119676632G>ACA378296590BAG3c.1078G>A (p.Glu360Lys)
c.901G>A (p.Glu301Lys)
c.1075G>A (p.Glu359Lys)
10g.119676632G>CCA378296591BAG3c.1078G>C (p.Glu360Gln)
c.901G>C (p.Glu301Gln)
c.1075G>C (p.Glu359Gln)
ClinVar dbSNP
10g.119676632G>TCA378296592BAG3c.1078G>T (p.Glu360Ter)
c.901G>T (p.Glu301Ter)
c.1075G>T (p.Glu359Ter)
COSMIC
10g.119676633A>CCA378296593BAG3c.1079A>C (p.Glu360Ala)
c.902A>C (p.Glu301Ala)
c.1076A>C (p.Glu359Ala)
10g.119676633A>GCA378296594BAG3c.1079A>G (p.Glu360Gly)
c.902A>G (p.Glu301Gly)
c.1076A>G (p.Glu359Gly)
10g.119676633A>TCA378296595BAG3c.1079A>T (p.Glu360Val)
c.902A>T (p.Glu301Val)
c.1076A>T (p.Glu359Val)

Number of alleles fetched