Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119670131_119670142delCA2611159847BAG3c.461_472del (p.Val154_Ala157del)
c.287_298del (p.Val96_Ala99del)
 gnomAD v4
10g.119670144_119670146dupCA282470BAG3c.474_476dup (p.Ala159_Ala160insAla)
c.300_302dup (p.Ala101_Ala102insAla)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670144_119670146delCA912966568BAG3c.474_476del (p.Ala159del)
c.300_302del (p.Ala101del)
 ClinVar dbSNP gnomAD v4
10g.119670141G>ACA175291BAG3c.471G>A (p.Ala157=)
c.297G>A (p.Ala99=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670141G>CCA471634598BAG3c.471G>C (p.Ala157=)
c.297G>C (p.Ala99=)
10g.119670141G=CA1940191290BAG3c.471G= (p.Ala157=)
c.297G= (p.Ala99=)
10g.119670141G>TCA471634599BAG3c.471G>T (p.Ala157=)
c.297G>T (p.Ala99=)
10g.119670142G>ACA378295159BAG3c.472G>A (p.Ala158Thr)
c.298G>A (p.Ala100Thr)
10g.119670142G>CCA378295157BAG3c.472G>C (p.Ala158Pro)
c.298G>C (p.Ala100Pro)
10g.119670142G>TCA378295158BAG3c.472G>T (p.Ala158Ser)
c.298G>T (p.Ala100Ser)
10g.119670143C>ACA378295160BAG3c.473C>A (p.Ala158Glu)
c.299C>A (p.Ala100Glu)
10g.119670143C=CA1940191298BAG3c.473C= (p.Ala158=)
c.299C= (p.Ala100=)
10g.119670143C>GCA378295161BAG3c.473C>G (p.Ala158Gly)
c.299C>G (p.Ala100Gly)
10g.119670143C>TCA5716328BAG3c.473C>T (p.Ala158Val)
c.299C>T (p.Ala100Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670144G>ACA214220178BAG3c.474G>A (p.Ala158=)
c.300G>A (p.Ala100=)
 ClinVar dbSNP gnomAD v4
10g.119670144G>CCA471634600BAG3c.474G>C (p.Ala158=)
c.300G>C (p.Ala100=)
10g.119670144G=CA1940191303BAG3c.474G= (p.Ala158=)
c.300G= (p.Ala100=)
10g.119670144G>TCA471634601BAG3c.474G>T (p.Ala158=)
c.300G>T (p.Ala100=)
10g.119670144_119670145dupCA918774547BAG3c.474_475dup (p.Ala159GlyfsTer?)
c.300_301dup (p.Ala101GlyfsTer?)
 dbSNP
10g.119670145G>ACA378295163BAG3c.475G>A (p.Ala159Thr)
c.301G>A (p.Ala101Thr)
 dbSNP gnomAD v2 gnomAD v4
10g.119670145G>CCA378295162BAG3c.475G>C (p.Ala159Pro)
c.301G>C (p.Ala101Pro)
10g.119670145G=CA1940191307BAG3c.475G= (p.Ala159=)
c.301G= (p.Ala101=)
10g.119670145G>TCA378295164BAG3c.475G>T (p.Ala159Ser)
c.301G>T (p.Ala101Ser)
10g.119670145_119670146delinsGCCA1940191306BAG3c.475_476delinsGC (p.Ala159=)
c.301_302delinsGC (p.Ala101=)
10g.119670147_119670149dupCA214220180BAG3c.477_479dup (p.Ala160_Gln161insAla)
c.303_305dup (p.Ala102_Gln103insAla)
 ClinVar dbSNP
10g.119670146delCA918774548BAG3c.476del (p.Ala159GlufsTer?)
c.302del (p.Ala101GlufsTer?)
 dbSNP
10g.119670146C>ACA378295165BAG3c.476C>A (p.Ala159Glu)
c.302C>A (p.Ala101Glu)
10g.119670146C>GCA378295167BAG3c.476C>G (p.Ala159Gly)
c.302C>G (p.Ala101Gly)
10g.119670146C>TCA378295166BAG3c.476C>T (p.Ala159Val)
c.302C>T (p.Ala101Val)
10g.119670147A>CCA471634602BAG3c.477A>C (p.Ala159=)
c.303A>C (p.Ala101=)
 dbSNP
10g.119670147A>GCA471634603BAG3c.477A>G (p.Ala159=)
c.303A>G (p.Ala101=)
10g.119670147A>TCA471634604BAG3c.477A>T (p.Ala159=)
c.303A>T (p.Ala101=)
10g.119670148G>ACA378295168BAG3c.478G>A (p.Ala160Thr)
c.304G>A (p.Ala102Thr)
 ClinVar
10g.119670148G>CCA378295170BAG3c.478G>C (p.Ala160Pro)
c.304G>C (p.Ala102Pro)
10g.119670148G>TCA378295169BAG3c.478G>T (p.Ala160Ser)
c.304G>T (p.Ala102Ser)
 gnomAD v4
10g.119670149C>ACA378295171BAG3c.479C>A (p.Ala160Asp)
c.305C>A (p.Ala102Asp)
10g.119670149C=CA1940191315BAG3c.479C= (p.Ala160=)
c.305C= (p.Ala102=)
10g.119670149C>GCA378295172BAG3c.479C>G (p.Ala160Gly)
c.305C>G (p.Ala102Gly)
10g.119670149C>TCA5716329BAG3c.479C>T (p.Ala160Val)
c.305C>T (p.Ala102Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670150_119670151delCA645568590BAG3c.480_481del (p.Gln161AlafsTer8)
c.306_307del (p.Gln103AlafsTer8)
 COSMIC
10g.119670150C>ACA471634606BAG3c.480C>A (p.Ala160=)
c.306C>A (p.Ala102=)
10g.119670150C=CA1940191319BAG3c.480C= (p.Ala160=)
c.306C= (p.Ala102=)
10g.119670150C>GCA471634607BAG3c.480C>G (p.Ala160=)
c.306C>G (p.Ala102=)
10g.119670150C>TCA5716330BAG3c.480C>T (p.Ala160=)
c.306C>T (p.Ala102=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670151C>ACA378295173BAG3c.481C>A (p.Gln161Lys)
c.307C>A (p.Gln103Lys)
10g.119670151C=CA1940191323BAG3c.481C= (p.Gln161=)
c.307C= (p.Gln103=)
10g.119670151C>GCA378295174BAG3c.481C>G (p.Gln161Glu)
c.307C>G (p.Gln103Glu)
10g.119670151C>TCA10587694BAG3c.481C>T (p.Gln161Ter)
c.307C>T (p.Gln103Ter)
 ClinVar dbSNP
10g.119670152A=CA1940191328BAG3c.482A= (p.Gln161=)
c.308A= (p.Gln103=)
10g.119670152A>CCA378295175BAG3c.482A>C (p.Gln161Pro)
c.308A>C (p.Gln103Pro)
10g.119670152A>GCA378295176BAG3c.482A>G (p.Gln161Arg)
c.308A>G (p.Gln103Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119670152A>TCA378295177BAG3c.482A>T (p.Gln161Leu)
c.308A>T (p.Gln103Leu)
10g.119670153G>ACA5716331BAG3c.483G>A (p.Gln161=)
c.309G>A (p.Gln103=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670153G>CCA378295178BAG3c.483G>C (p.Gln161His)
c.309G>C (p.Gln103His)
10g.119670153G=CA1940191330BAG3c.483G= (p.Gln161=)
c.309G= (p.Gln103=)
10g.119670153G>TCA378295179BAG3c.483G>T (p.Gln161His)
c.309G>T (p.Gln103His)
10g.119670153_119670154delinsGCCA1940191329BAG3c.483_484delinsGC (p.Gln161=)
c.309_310delinsGC (p.Gln103=)
10g.119670154C>ACA378295180BAG3c.484C>A (p.Pro162Thr)
c.310C>A (p.Pro104Thr)
 ClinVar dbSNP gnomAD v4
10g.119670154C>GCA378295181BAG3c.484C>G (p.Pro162Ala)
c.310C>G (p.Pro104Ala)
10g.119670154C>TCA378295182BAG3c.484C>T (p.Pro162Ser)
c.310C>T (p.Pro104Ser)
 ClinVar dbSNP gnomAD v4
10g.119670158dupCA2611159848BAG3c.488dup (p.Ala164SerfsTer6)
c.314dup (p.Ala106SerfsTer6)
 gnomAD v4
10g.119670158delCA933132626BAG3c.488del (p.Pro163GlnfsTer?)
c.314del (p.Pro105GlnfsTer?)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119670155C>ACA378295183BAG3c.485C>A (p.Pro162His)
c.311C>A (p.Pro104His)
10g.119670155C=CA1940191332BAG3c.485C= (p.Pro162=)
c.311C= (p.Pro104=)
10g.119670155C>GCA378295184BAG3c.485C>G (p.Pro162Arg)
c.311C>G (p.Pro104Arg)
10g.119670155C>TCA5716332BAG3c.485C>T (p.Pro162Leu)
c.311C>T (p.Pro104Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670156C>ACA471634608BAG3c.486C>A (p.Pro162=)
c.312C>A (p.Pro104=)
10g.119670156C>GCA471634609BAG3c.486C>G (p.Pro162=)
c.312C>G (p.Pro104=)
10g.119670156C>TCA471634610BAG3c.486C>T (p.Pro162=)
c.312C>T (p.Pro104=)
10g.119670157C>ACA378295185BAG3c.487C>A (p.Pro163Thr)
c.313C>A (p.Pro105Thr)
10g.119670157C=CA1940191337BAG3c.487C= (p.Pro163=)
c.313C= (p.Pro105=)
10g.119670157C>GCA378295186BAG3c.487C>G (p.Pro163Ala)
c.313C>G (p.Pro105Ala)
10g.119670157C>TCA241532BAG3c.487C>T (p.Pro163Ser)
c.313C>T (p.Pro105Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670158C>ACA378295187BAG3c.488C>A (p.Pro163Gln)
c.314C>A (p.Pro105Gln)
10g.119670158C>GCA378295188BAG3c.488C>G (p.Pro163Arg)
c.314C>G (p.Pro105Arg)
10g.119670158C>TCA378295189BAG3c.488C>T (p.Pro163Leu)
c.314C>T (p.Pro105Leu)
10g.119670159A>CCA471634611BAG3c.489A>C (p.Pro163=)
c.315A>C (p.Pro105=)
 dbSNP
10g.119670159A>GCA471634612BAG3c.489A>G (p.Pro163=)
c.315A>G (p.Pro105=)
10g.119670159A>TCA471634613BAG3c.489A>T (p.Pro163=)
c.315A>T (p.Pro105=)
10g.119670160G>ACA378295190BAG3c.490G>A (p.Ala164Thr)
c.316G>A (p.Ala106Thr)
 dbSNP gnomAD v4
10g.119670160G>CCA378295191BAG3c.490G>C (p.Ala164Pro)
c.316G>C (p.Ala106Pro)
 gnomAD v4
10g.119670160G=CA1940191339BAG3c.490G= (p.Ala164=)
c.316G= (p.Ala106=)
10g.119670160G>TCA378295192BAG3c.490G>T (p.Ala164Ser)
c.316G>T (p.Ala106Ser)
 ClinVar gnomAD v4
10g.119670161C>ACA378295195BAG3c.491C>A (p.Ala164Asp)
c.317C>A (p.Ala106Asp)
10g.119670161C>GCA378295194BAG3c.491C>G (p.Ala164Gly)
c.317C>G (p.Ala106Gly)
10g.119670161C>TCA378295193BAG3c.491C>T (p.Ala164Val)
c.317C>T (p.Ala106Val)
10g.119670162C>ACA471634617BAG3c.492C>A (p.Ala164=)
c.318C>A (p.Ala106=)
10g.119670162C>GCA471634618BAG3c.492C>G (p.Ala164=)
c.318C>G (p.Ala106=)
10g.119670162C>TCA471634619BAG3c.492C>T (p.Ala164=)
c.318C>T (p.Ala106=)
 gnomAD v4
10g.119670163T>ACA378295196BAG3c.493T>A (p.Ser165Thr)
c.319T>A (p.Ser107Thr)
10g.119670163T>CCA378295197BAG3c.493T>C (p.Ser165Pro)
c.319T>C (p.Ser107Pro)
10g.119670163T>GCA378295198BAG3c.493T>G (p.Ser165Ala)
c.319T>G (p.Ser107Ala)
10g.119670164C>ACA378295199BAG3c.494C>A (p.Ser165Tyr)
c.320C>A (p.Ser107Tyr)
10g.119670164C=CA1940191342BAG3c.494C= (p.Ser165=)
c.320C= (p.Ser107=)
10g.119670164C>GCA378295200BAG3c.494C>G (p.Ser165Cys)
c.320C>G (p.Ser107Cys)
10g.119670164C>TCA5716333BAG3c.494C>T (p.Ser165Phe)
c.320C>T (p.Ser107Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670165C>ACA471634621BAG3c.495C>A (p.Ser165=)
c.321C>A (p.Ser107=)
10g.119670165C=CA1940191344BAG3c.495C= (p.Ser165=)
c.321C= (p.Ser107=)
10g.119670165C>GCA5716334BAG3c.495C>G (p.Ser165=)
c.321C>G (p.Ser107=)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670165C>TCA214220272BAG3c.495C>T (p.Ser165=)
c.321C>T (p.Ser107=)
 ClinVar dbSNP gnomAD v4
10g.119670166C>ACA378295201BAG3c.496C>A (p.His166Asn)
c.322C>A (p.His108Asn)
10g.119670166C>GCA378295202BAG3c.496C>G (p.His166Asp)
c.322C>G (p.His108Asp)
10g.119670166C>TCA378295203BAG3c.496C>T (p.His166Tyr)
c.322C>T (p.His108Tyr)
10g.119670167A>CCA378295206BAG3c.497A>C (p.His166Pro)
c.323A>C (p.His108Pro)
10g.119670167A>GCA378295205BAG3c.497A>G (p.His166Arg)
c.323A>G (p.His108Arg)
10g.119670167A>TCA378295204BAG3c.497A>T (p.His166Leu)
c.323A>T (p.His108Leu)
10g.119670168C>ACA378295207BAG3c.498C>A (p.His166Gln)
c.324C>A (p.His108Gln)
10g.119670168C=CA1940191350BAG3c.498C= (p.His166=)
c.324C= (p.His108=)
10g.119670168C>GCA378295208BAG3c.498C>G (p.His166Gln)
c.324C>G (p.His108Gln)
10g.119670168C>TCA5716335BAG3c.498C>T (p.His166=)
c.324C>T (p.His108=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670169G>ACA5716336BAG3c.499G>A (p.Gly167Arg)
c.325G>A (p.Gly109Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670169G>CCA378295209BAG3c.499G>C (p.Gly167Arg)
c.325G>C (p.Gly109Arg)
10g.119670169G=CA1940191353BAG3c.499G= (p.Gly167=)
c.325G= (p.Gly109=)
10g.119670169G>TCA378295210BAG3c.499G>T (p.Gly167Ter)
c.325G>T (p.Gly109Ter)
10g.119670170G>ACA378295211BAG3c.500G>A (p.Gly167Glu)
c.326G>A (p.Gly109Glu)
10g.119670170G>CCA378295212BAG3c.500G>C (p.Gly167Ala)
c.326G>C (p.Gly109Ala)
10g.119670170G>TCA378295213BAG3c.500G>T (p.Gly167Val)
c.326G>T (p.Gly109Val)
10g.119670171A=CA1940191358BAG3c.501A= (p.Gly167=)
c.327A= (p.Gly109=)
10g.119670171A>CCA471634624BAG3c.501A>C (p.Gly167=)
c.327A>C (p.Gly109=)
10g.119670171A>GCA471634625BAG3c.501A>G (p.Gly167=)
c.327A>G (p.Gly109=)
 ClinVar dbSNP
10g.119670171A>TCA471634626BAG3c.501A>T (p.Gly167=)
c.327A>T (p.Gly109=)
10g.119670172C>ACA378295214BAG3c.502C>A (p.Pro168Thr)
c.328C>A (p.Pro110Thr)
10g.119670172C=CA1940191362BAG3c.502C= (p.Pro168=)
c.328C= (p.Pro110=)
10g.119670172C>GCA378295215BAG3c.502C>G (p.Pro168Ala)
c.328C>G (p.Pro110Ala)
 gnomAD v4
10g.119670172C>TCA378295216BAG3c.502C>T (p.Pro168Ser)
c.328C>T (p.Pro110Ser)
 ClinVar dbSNP gnomAD v4
10g.119670173C>ACA378295218BAG3c.503C>A (p.Pro168His)
c.329C>A (p.Pro110His)
10g.119670173C=CA1940191365BAG3c.503C= (p.Pro168=)
c.329C= (p.Pro110=)
10g.119670173C>GCA378295217BAG3c.503C>G (p.Pro168Arg)
c.329C>G (p.Pro110Arg)
 gnomAD v4
10g.119670173C>TCA214220291BAG3c.503C>T (p.Pro168Leu)
c.329C>T (p.Pro110Leu)
 dbSNP gnomAD v3 gnomAD v4
10g.119670174T>ACA471634628BAG3c.504T>A (p.Pro168=)
c.330T>A (p.Pro110=)
10g.119670174T>CCA471634629BAG3c.504T>C (p.Pro168=)
c.330T>C (p.Pro110=)
10g.119670174T>GCA471634630BAG3c.504T>G (p.Pro168=)
c.330T>G (p.Pro110=)
10g.119670175G>ACA378295219BAG3c.505G>A (p.Glu169Lys)
c.331G>A (p.Glu111Lys)
10g.119670175G>CCA378295221BAG3c.505G>C (p.Glu169Gln)
c.331G>C (p.Glu111Gln)
10g.119670175G>TCA378295220BAG3c.505G>T (p.Glu169Ter)
c.331G>T (p.Glu111Ter)
10g.119670176A>CCA378295222BAG3c.506A>C (p.Glu169Ala)
c.332A>C (p.Glu111Ala)
10g.119670176A>GCA378295223BAG3c.506A>G (p.Glu169Gly)
c.332A>G (p.Glu111Gly)
 gnomAD v4
10g.119670176A>TCA378295224BAG3c.506A>T (p.Glu169Val)
c.332A>T (p.Glu111Val)
10g.119670177G>ACA471634632BAG3c.507G>A (p.Glu169=)
c.333G>A (p.Glu111=)
10g.119670177G>CCA16612844BAG3c.507G>C (p.Glu169Asp)
c.333G>C (p.Glu111Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119670177G=CA1940191367BAG3c.507G= (p.Glu169=)
c.333G= (p.Glu111=)
10g.119670177G>TCA378295225BAG3c.507G>T (p.Glu169Asp)
c.333G>T (p.Glu111Asp)
10g.119670178G>ACA378295226BAG3c.507+1G>A (n.507+1G>A)
c.333+1G>A (n.333+1G>A)
10g.119670178G>CCA378295227BAG3c.507+1G>C (n.507+1G>C)
c.333+1G>C (n.333+1G>C)
10g.119670178G>TCA378295228BAG3c.507+1G>T (n.507+1G>T)
c.333+1G>T (n.333+1G>T)
 gnomAD v4
10g.119670179T>ACA378295229BAG3c.507+2T>A (n.507+2T>A)
c.333+2T>A (n.333+2T>A)
10g.119670179T>CCA378295230BAG3c.507+2T>C (n.507+2T>C)
c.333+2T>C (n.333+2T>C)
10g.119670179T>GCA378295231BAG3c.507+2T>G (n.507+2T>G)
c.333+2T>G (n.333+2T>G)
 dbSNP
10g.119670181A>GCA2611159849BAG3c.507+4A>G (n.507+4A>G)
c.333+4A>G (n.333+4A>G)
 gnomAD v4
10g.119670182G>ACA2580082419BAG3c.507+5G>A (n.507+5G>A)
c.333+5G>A (n.333+5G>A)
 ClinVar gnomAD v4
10g.119670182G>TCA2611159850BAG3c.507+5G>T (n.507+5G>T)
c.333+5G>T (n.333+5G>T)
 gnomAD v4
10g.119670184A>GCA2499220170BAG3c.507+7A>G (n.507+7A>G)
c.333+7A>G (n.333+7A>G)
 ClinVar dbSNP
10g.119670184_119670228delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTTCA1940191369BAG3c.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT (n.507+7_507+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT)
c.333+7_333+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT (n.333+7_333+51delinsAGAGGCCAGGCTCACCAGCCTGCTGGGGAGCAAGCCGCTGTGCTT)
10g.119670185G>TCA2611159851BAG3c.507+8G>T (n.507+8G>T)
c.333+8G>T (n.333+8G>T)
 gnomAD v4
10g.119670185_119670228delCA5716337BAG3c.507+8_507+51del (n.507+8_507+51del)
c.333+8_333+51del (n.333+8_333+51del)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670187G>ACA214220301BAG3c.507+10G>A (n.507+10G>A)
c.333+10G>A (n.333+10G>A)
 ClinVar dbSNP
10g.119670187G=CA1940191373BAG3c.507+10G= (n.507+10G=)
c.333+10G= (n.333+10G=)
10g.119670191A>CCA2611159852BAG3c.507+14A>C (n.507+14A>C)
c.333+14A>C (n.333+14A>C)
 gnomAD v4
10g.119670192G>CCA5716338BAG3c.507+15G>C (n.507+15G>C)
c.333+15G>C (n.333+15G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670192G=CA1940191377BAG3c.507+15G= (n.507+15G=)
c.333+15G= (n.333+15G=)
10g.119670192G>TCA2611159853BAG3c.507+15G>T (n.507+15G>T)
c.333+15G>T (n.333+15G>T)
 gnomAD v4
10g.119670192_119670216delinsGGCTCACCAGCCTGCTGGGGAGCAACA1940191375BAG3c.507+15_507+39delinsGGCTCACCAGCCTGCTGGGGAGCAA (n.507+15_507+39delinsGGCTCACCAGCCTGCTGGGGAGCAA)
c.333+15_333+39delinsGGCTCACCAGCCTGCTGGGGAGCAA (n.333+15_333+39delinsGGCTCACCAGCCTGCTGGGGAGCAA)
10g.119670193G>ACA5716340BAG3c.507+16G>A (n.507+16G>A)
c.333+16G>A (n.333+16G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670193G=CA1940191380BAG3c.507+16G= (n.507+16G=)
c.333+16G= (n.333+16G=)
10g.119670193G>TCA660663569BAG3c.507+16G>T (n.507+16G>T)
c.333+16G>T (n.333+16G>T)
 dbSNP gnomAD v3 gnomAD v4
10g.119670195_119670218delCA5716339BAG3c.507+18_507+41del (n.507+18_507+41del)
c.333+18_333+41del (n.333+18_333+41del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670194C>ACA2611159854BAG3c.507+17C>A (n.507+17C>A)
c.333+17C>A (n.333+17C>A)
 gnomAD v4
10g.119670194C>TCA2499220171BAG3c.507+17C>T (n.507+17C>T)
c.333+17C>T (n.333+17C>T)
 ClinVar dbSNP
10g.119670195T>CCA289664BAG3c.507+18T>C (n.507+18T>C)
c.333+18T>C (n.333+18T>C)
 ClinVar dbSNP gnomAD v4
10g.119670195T=CA1940191384BAG3c.507+18T= (n.507+18T=)
c.333+18T= (n.333+18T=)
10g.119670196C>ACA2611159855BAG3c.507+19C>A (n.507+19C>A)
c.333+19C>A (n.333+19C>A)
 gnomAD v4
10g.119670196C>TCA2539184080BAG3c.507+19C>T (n.507+19C>T)
c.333+19C>T (n.333+19C>T)
 dbSNP gnomAD v4
10g.119670197A>CCA2574457113BAG3c.507+20A>C (n.507+20A>C)
c.333+20A>C (n.333+20A>C)
 gnomAD v4
10g.119670199C>ACA596325800BAG3c.507+22C>A (n.507+22C>A)
c.333+22C>A (n.333+22C>A)
 dbSNP gnomAD v2 gnomAD v4
10g.119670199C=CA1940191388BAG3c.507+22C= (n.507+22C=)
c.333+22C= (n.333+22C=)
10g.119670199C>TCA2611159856BAG3c.507+22C>T (n.507+22C>T)
c.333+22C>T (n.333+22C>T)
 gnomAD v4
10g.119670201G>ACA2611159857BAG3c.507+24G>A (n.507+24G>A)
c.333+24G>A (n.333+24G>A)
 gnomAD v4
10g.119670201G>TCA2611159858BAG3c.507+24G>T (n.507+24G>T)
c.333+24G>T (n.333+24G>T)
 gnomAD v4
10g.119670202C>ACA2611159859BAG3c.507+25C>A (n.507+25C>A)
c.333+25C>A (n.333+25C>A)
 gnomAD v4
10g.119670202C>TCA2611159860BAG3c.507+25C>T (n.507+25C>T)
c.333+25C>T (n.333+25C>T)
 gnomAD v4
10g.119670203C>ACA2532052845BAG3c.507+26C>A (n.507+26C>A)
c.333+26C>A (n.333+26C>A)
 gnomAD v4
10g.119670203_119670204delinsCTCA1940191390BAG3c.507+26_507+27delinsCT (n.507+26_507+27delinsCT)
c.333+26_333+27delinsCT (n.333+26_333+27delinsCT)
10g.119670204delCA5716341BAG3c.507+27del (n.507+27del)
c.333+27del (n.333+27del)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670204T>GCA2574457114BAG3c.507+27T>G (n.507+27T>G)
c.333+27T>G (n.333+27T>G)
 gnomAD v4
10g.119670205G>ACA2611159861BAG3c.507+28G>A (n.507+28G>A)
c.333+28G>A (n.333+28G>A)
 gnomAD v4
10g.119670205G>CCA2574457115BAG3c.507+28G>C (n.507+28G>C)
c.333+28G>C (n.333+28G>C)
10g.119670205G>TCA2611159862BAG3c.507+28G>T (n.507+28G>T)
c.333+28G>T (n.333+28G>T)
 gnomAD v4
10g.119670206C>ACA2611159863BAG3c.507+29C>A (n.507+29C>A)
c.333+29C>A (n.333+29C>A)
 gnomAD v4
10g.119670206C=CA1940191392BAG3c.507+29C= (n.507+29C=)
c.333+29C= (n.333+29C=)
10g.119670206C>GCA596325802BAG3c.507+29C>G (n.507+29C>G)
c.333+29C>G (n.333+29C>G)
 dbSNP gnomAD v2 gnomAD v4
10g.119670206C>TCA596325803BAG3c.507+29C>T (n.507+29C>T)
c.333+29C>T (n.333+29C>T)
 dbSNP gnomAD v2 gnomAD v4
10g.119670207T>CCA1940191396BAG3c.507+30T>C (n.507+30T>C)
c.333+30T>C (n.333+30T>C)
 dbSNP gnomAD v4
10g.119670207T>GCA5716342BAG3c.507+30T>G (n.507+30T>G)
c.333+30T>G (n.333+30T>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670207T=CA1940191395BAG3c.507+30T= (n.507+30T=)
c.333+30T= (n.333+30T=)
10g.119670208G>ACA1940191400BAG3c.507+31G>A (n.507+31G>A)
c.333+31G>A (n.333+31G>A)
 dbSNP gnomAD v3 gnomAD v4
10g.119670208G=CA1940191398BAG3c.507+31G= (n.507+31G=)
c.333+31G= (n.333+31G=)
10g.119670208G>TCA2611159865BAG3c.507+31G>T (n.507+31G>T)
c.333+31G>T (n.333+31G>T)
 gnomAD v4
10g.119670211dupCA2611159864BAG3c.507+34dup (n.507+34dup)
c.333+34dup (n.333+34dup)
 gnomAD v4
10g.119670211delCA2574457116BAG3c.507+34del (n.507+34del)
c.333+34del (n.333+34del)
 gnomAD v4
10g.119670209G>ACA2611159866BAG3c.507+32G>A (n.507+32G>A)
c.333+32G>A (n.333+32G>A)
 gnomAD v4
10g.119670209G>TCA2611159867BAG3c.507+32G>T (n.507+32G>T)
c.333+32G>T (n.333+32G>T)
 gnomAD v4
10g.119670210G>ACA2611159868BAG3c.507+33G>A (n.507+33G>A)
c.333+33G>A (n.333+33G>A)
 gnomAD v4
10g.119670210G>TCA2574457117BAG3c.507+33G>T (n.507+33G>T)
c.333+33G>T (n.333+33G>T)
 gnomAD v4
10g.119670211G>ACA1940191403BAG3c.507+34G>A (n.507+34G>A)
c.333+34G>A (n.333+34G>A)
 dbSNP gnomAD v4
10g.119670211G=CA1940191401BAG3c.507+34G= (n.507+34G=)
c.333+34G= (n.333+34G=)
10g.119670213G>ACA1940191408BAG3c.507+36G>A (n.507+36G>A)
c.333+36G>A (n.333+36G>A)
 dbSNP gnomAD v4
10g.119670213G>CCA5716343BAG3c.507+36G>C (n.507+36G>C)
c.333+36G>C (n.333+36G>C)
 dbSNP ExAC gnomAD v4
10g.119670213G=CA1940191406BAG3c.507+36G= (n.507+36G=)
c.333+36G= (n.333+36G=)
10g.119670214C>ACA5716344BAG3c.507+37C>A (n.507+37C>A)
c.333+37C>A (n.333+37C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670214C=CA1940191410BAG3c.507+37C= (n.507+37C=)
c.333+37C= (n.333+37C=)
10g.119670214C>TCA596325806BAG3c.507+37C>T (n.507+37C>T)
c.333+37C>T (n.333+37C>T)
 dbSNP gnomAD v2 gnomAD v4
10g.119670215A>CCA2611159869BAG3c.507+38A>C (n.507+38A>C)
c.333+38A>C (n.333+38A>C)
 gnomAD v4
10g.119670215_119670220delCA2611159870BAG3c.507+38_507+43del (n.507+38_507+43del)
c.333+38_333+43del (n.333+38_333+43del)
 gnomAD v4
10g.119670216A=CA1940191411BAG3c.507+39A= (n.507+39A=)
c.333+39A= (n.333+39A=)
10g.119670216A>CCA214220357BAG3c.507+39A>C (n.507+39A>C)
c.333+39A>C (n.333+39A>C)
 dbSNP gnomAD v3 gnomAD v4
10g.119670216A>TCA2611159871BAG3c.507+39A>T (n.507+39A>T)
c.333+39A>T (n.333+39A>T)
 gnomAD v4
10g.119670217G>ACA2611159872BAG3c.507+40G>A (n.507+40G>A)
c.333+40G>A (n.333+40G>A)
 gnomAD v4
10g.119670217G>TCA2611159873BAG3c.507+40G>T (n.507+40G>T)
c.333+40G>T (n.333+40G>T)
 gnomAD v4
10g.119670218C>ACA2611159874BAG3c.507+41C>A (n.507+41C>A)
c.333+41C>A (n.333+41C>A)
 gnomAD v4
10g.119670218C=CA1940191413BAG3c.507+41C= (n.507+41C=)
c.333+41C= (n.333+41C=)
10g.119670218C>GCA2611159875BAG3c.507+41C>G (n.507+41C>G)
c.333+41C>G (n.333+41C>G)
 gnomAD v4
10g.119670218C>TCA5716345BAG3c.507+41C>T (n.507+41C>T)
c.333+41C>T (n.333+41C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670219C>ACA2611159876BAG3c.507+42C>A (n.507+42C>A)
c.333+42C>A (n.333+42C>A)
 gnomAD v4
10g.119670219C=CA1940191415BAG3c.507+42C= (n.507+42C=)
c.333+42C= (n.333+42C=)
10g.119670219C>GCA933132664BAG3c.507+42C>G (n.507+42C>G)
c.333+42C>G (n.333+42C>G)
 dbSNP gnomAD v3 gnomAD v4
10g.119670219C>TCA5716346BAG3c.507+42C>T (n.507+42C>T)
c.333+42C>T (n.333+42C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670220G>ACA5716347BAG3c.507+43G>A (n.507+43G>A)
c.333+43G>A (n.333+43G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670220G=CA1940191418BAG3c.507+43G= (n.507+43G=)
c.333+43G= (n.333+43G=)
10g.119670220G>TCA660663597BAG3c.507+43G>T (n.507+43G>T)
c.333+43G>T (n.333+43G>T)
 dbSNP gnomAD v3 gnomAD v4
10g.119670221C=CA1940191420BAG3c.507+44C= (n.507+44C=)
c.333+44C= (n.333+44C=)
10g.119670221C>TCA5716348BAG3c.507+44C>T (n.507+44C>T)
c.333+44C>T (n.333+44C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670223G>ACA2611159878BAG3c.507+46G>A (n.507+46G>A)
c.333+46G>A (n.333+46G>A)
 gnomAD v4
10g.119670223G>TCA2574457118BAG3c.507+46G>T (n.507+46G>T)
c.333+46G>T (n.333+46G>T)
 gnomAD v4
10g.119670224_119670233delCA2611159877BAG3c.507+47_507+56del (n.507+47_507+56del)
c.333+47_333+56del (n.333+47_333+56del)
 gnomAD v4
10g.119670224T>CCA2611159879BAG3c.507+47T>C (n.507+47T>C)
c.333+47T>C (n.333+47T>C)
 gnomAD v4
10g.119670225G>ACA1940191424BAG3c.507+48G>A (n.507+48G>A)
c.333+48G>A (n.333+48G>A)
 dbSNP gnomAD v4
10g.119670225G=CA1940191423BAG3c.507+48G= (n.507+48G=)
c.333+48G= (n.333+48G=)
10g.119670225G>TCA2611159880BAG3c.507+48G>T (n.507+48G>T)
c.333+48G>T (n.333+48G>T)
 gnomAD v4
10g.119670226C>ACA2611159881BAG3c.507+49C>A (n.507+49C>A)
c.333+49C>A (n.333+49C>A)
 gnomAD v4
10g.119670226C>TCA2611159882BAG3c.507+49C>T (n.507+49C>T)
c.333+49C>T (n.333+49C>T)
 gnomAD v4
10g.119670228T>CCA5716349BAG3c.507+51T>C (n.507+51T>C)
c.333+51T>C (n.333+51T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670228T=CA1940191425BAG3c.507+51T= (n.507+51T=)
c.333+51T= (n.333+51T=)
10g.119670229C>ACA2611159884BAG3c.507+52C>A (n.507+52C>A)
c.333+52C>A (n.333+52C>A)
 gnomAD v4
10g.119670229C>TCA2611159885BAG3c.507+52C>T (n.507+52C>T)
c.333+52C>T (n.333+52C>T)
 gnomAD v4
10g.119670231delCA2611159883BAG3c.507+54del (n.507+54del)
c.333+54del (n.333+54del)
 gnomAD v4
10g.119670230C>ACA2611159886BAG3c.507+53C>A (n.507+53C>A)
c.333+53C>A (n.333+53C>A)
 gnomAD v4
10g.119670230C=CA1940191428BAG3c.507+53C= (n.507+53C=)
c.333+53C= (n.333+53C=)
10g.119670230C>GCA2611159887BAG3c.507+53C>G (n.507+53C>G)
c.333+53C>G (n.333+53C>G)
 gnomAD v4
10g.119670230C>TCA660663601BAG3c.507+53C>T (n.507+53C>T)
c.333+53C>T (n.333+53C>T)
 dbSNP gnomAD v3 gnomAD v4
10g.119670231C>ACA660663604BAG3c.507+54C>A (n.507+54C>A)
c.333+54C>A (n.333+54C>A)
 dbSNP gnomAD v3 gnomAD v4
10g.119670231C=CA1940191430BAG3c.507+54C= (n.507+54C=)
c.333+54C= (n.333+54C=)
10g.119670231C>GCA2611159888BAG3c.507+54C>G (n.507+54C>G)
c.333+54C>G (n.333+54C>G)
 gnomAD v4
10g.119670231C>TCA2611159889BAG3c.507+54C>T (n.507+54C>T)
c.333+54C>T (n.333+54C>T)
 gnomAD v4
10g.119670232A>GCA2611159890BAG3c.507+55A>G (n.507+55A>G)
c.333+55A>G (n.333+55A>G)
 gnomAD v4
10g.119670233G>ACA2611159892BAG3c.507+56G>A (n.507+56G>A)
c.333+56G>A (n.333+56G>A)
 gnomAD v4
10g.119670233G>CCA2611159891BAG3c.507+56G>C (n.507+56G>C)
c.333+56G>C (n.333+56G>C)
 gnomAD v4
10g.119670233G=CA1940191432BAG3c.507+56G= (n.507+56G=)
c.333+56G= (n.333+56G=)
10g.119670233G>TCA660663605BAG3c.507+56G>T (n.507+56G>T)
c.333+56G>T (n.333+56G>T)
 dbSNP gnomAD v4
10g.119670234G>ACA2611159893BAG3c.507+57G>A (n.507+57G>A)
c.333+57G>A (n.333+57G>A)
 gnomAD v4
10g.119670234G>TCA2611159894BAG3c.507+57G>T (n.507+57G>T)
c.333+57G>T (n.333+57G>T)
 gnomAD v4
10g.119670235C>ACA2611159895BAG3c.507+58C>A (n.507+58C>A)
c.333+58C>A (n.333+58C>A)
 gnomAD v4
10g.119670235C=CA1940191437BAG3c.507+58C= (n.507+58C=)
c.333+58C= (n.333+58C=)
10g.119670235C>TCA214220404BAG3c.507+58C>T (n.507+58C>T)
c.333+58C>T (n.333+58C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119670236C>ACA2611159896BAG3c.507+59C>A (n.507+59C>A)
c.333+59C>A (n.333+59C>A)
 gnomAD v4
10g.119670236C=CA1940191440BAG3c.507+59C= (n.507+59C=)
c.333+59C= (n.333+59C=)
10g.119670236C>TCA660663608BAG3c.507+59C>T (n.507+59C>T)
c.333+59C>T (n.333+59C>T)
 dbSNP gnomAD v3 gnomAD v4
10g.119670237G>ACA214220409BAG3c.507+60G>A (n.507+60G>A)
c.333+60G>A (n.333+60G>A)
 dbSNP gnomAD v3 gnomAD v4
10g.119670237G=CA1940191442BAG3c.507+60G= (n.507+60G=)
c.333+60G= (n.333+60G=)
10g.119670237G>TCA2611159898BAG3c.507+60G>T (n.507+60G>T)
c.333+60G>T (n.333+60G>T)
 gnomAD v4
10g.119670239delCA2611159897BAG3c.507+62del (n.507+62del)
c.333+62del (n.333+62del)
 gnomAD v4
10g.119670238G>TCA2611159899BAG3c.507+61G>T (n.507+61G>T)
c.333+61G>T (n.333+61G>T)
 gnomAD v4
10g.119670239G>ACA2611159900BAG3c.507+62G>A (n.507+62G>A)
c.333+62G>A (n.333+62G>A)
 gnomAD v4
10g.119670239G=CA1940191445BAG3c.507+62G= (n.507+62G=)
c.333+62G= (n.333+62G=)
10g.119670239G>TCA660663618BAG3c.507+62G>T (n.507+62G>T)
c.333+62G>T (n.333+62G>T)
 dbSNP gnomAD v4
10g.119670240C>ACA2611159903BAG3c.507+63C>A (n.507+63C>A)
c.333+63C>A (n.333+63C>A)
 gnomAD v4
10g.119670240C=CA1940191448BAG3c.507+63C= (n.507+63C=)
c.333+63C= (n.333+63C=)
10g.119670240C>GCA2611159902BAG3c.507+63C>G (n.507+63C>G)
c.333+63C>G (n.333+63C>G)
 gnomAD v4
10g.119670240C>TCA660663625BAG3c.507+63C>T (n.507+63C>T)
c.333+63C>T (n.333+63C>T)
 dbSNP gnomAD v4
10g.119670242delCA2611159901BAG3c.507+65del (n.507+65del)
c.333+65del (n.333+65del)
 gnomAD v4
10g.119670241C>ACA2611159904BAG3c.507+64C>A (n.507+64C>A)
c.333+64C>A (n.333+64C>A)
 gnomAD v4

Number of alleles fetched