Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119674392_119683124delCA2580082473 ClinVar
10g.119675031_119678711delCA2580082474 ClinVar
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.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)
10g.119676634G>ACA471634919BAG3c.1080G>A (p.Glu360=)
c.903G>A (p.Glu301=)
c.1077G>A (p.Glu359=)

Number of alleles fetched