Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119674392_119683124delCA2580082473 ClinVar
10g.119675031_119678711delCA2580082474 ClinVar
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=)
10g.119676634G>CCA378296596BAG3c.1080G>C (p.Glu360Asp)
c.903G>C (p.Glu301Asp)
c.1077G>C (p.Glu359Asp)
10g.119676634G=CA1940196607BAG3c.1080G= (p.Glu360=)
c.903G= (p.Glu301=)
c.1077G= (p.Glu359=)
10g.119676634G>TCA378296597BAG3c.1080G>T (p.Glu360Asp)
c.903G>T (p.Glu301Asp)
c.1077G>T (p.Glu359Asp)
dbSNP gnomAD v2 gnomAD v4
10g.119676635A>CCA378296598BAG3c.1081A>C (p.Lys361Gln)
c.904A>C (p.Lys302Gln)
c.1078A>C (p.Lys360Gln)
10g.119676635A>GCA378296600BAG3c.1081A>G (p.Lys361Glu)
c.904A>G (p.Lys302Glu)
c.1078A>G (p.Lys360Glu)
10g.119676635A>TCA378296599BAG3c.1081A>T (p.Lys361Ter)
c.904A>T (p.Lys302Ter)
c.1078A>T (p.Lys360Ter)
10g.119676636A>CCA378296601BAG3c.1082A>C (p.Lys361Thr)
c.905A>C (p.Lys302Thr)
c.1079A>C (p.Lys360Thr)
10g.119676636A>GCA378296602BAG3c.1082A>G (p.Lys361Arg)
c.905A>G (p.Lys302Arg)
c.1079A>G (p.Lys360Arg)
10g.119676636A>TCA378296603BAG3c.1082A>T (p.Lys361Met)
c.905A>T (p.Lys302Met)
c.1079A>T (p.Lys360Met)
10g.119676637G>ACA16612747BAG3c.1083G>A (p.Lys361=)
c.906G>A (p.Lys302=)
c.1080G>A (p.Lys360=)
ClinVar dbSNP
10g.119676637G>CCA378296604BAG3c.1083G>C (p.Lys361Asn)
c.906G>C (p.Lys302Asn)
c.1080G>C (p.Lys360Asn)
ClinVar dbSNP gnomAD v4
10g.119676637G=CA1940196608BAG3c.1083G= (p.Lys361=)
c.906G= (p.Lys302=)
c.1080G= (p.Lys360=)
10g.119676637G>TCA378296605BAG3c.1083G>T (p.Lys361Asn)
c.906G>T (p.Lys302Asn)
c.1080G>T (p.Lys360Asn)
10g.119676638G>ACA214224867BAG3c.1084G>A (p.Val362Ile)
c.907G>A (p.Val303Ile)
c.1081G>A (p.Val361Ile)
ClinVar dbSNP
10g.119676638G>CCA378296606BAG3c.1084G>C (p.Val362Leu)
c.907G>C (p.Val303Leu)
c.1081G>C (p.Val361Leu)
10g.119676638G=CA1940196609BAG3c.1084G= (p.Val362=)
c.907G= (p.Val303=)
c.1081G= (p.Val361=)
10g.119676638G>TCA378296607BAG3c.1084G>T (p.Val362Leu)
c.907G>T (p.Val303Leu)
c.1081G>T (p.Val361Leu)
10g.119676639T>ACA378296608BAG3c.1085T>A (p.Val362Glu)
c.908T>A (p.Val303Glu)
c.1082T>A (p.Val361Glu)
10g.119676639T>CCA5716481BAG3c.1085T>C (p.Val362Ala)
c.908T>C (p.Val303Ala)
c.1082T>C (p.Val361Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119676639T>GCA378296609BAG3c.1085T>G (p.Val362Gly)
c.908T>G (p.Val303Gly)
c.1082T>G (p.Val361Gly)
10g.119676639T=CA1940196610BAG3c.1085T= (p.Val362=)
c.908T= (p.Val303=)
c.1082T= (p.Val361=)
10g.119676640A=CA1940196611BAG3c.1086A= (p.Val362=)
c.909A= (p.Val303=)
c.1083A= (p.Val361=)
10g.119676640A>CCA471634928BAG3c.1086A>C (p.Val362=)
c.909A>C (p.Val303=)
c.1083A>C (p.Val361=)
10g.119676640A>GCA471634929BAG3c.1086A>G (p.Val362=)
c.909A>G (p.Val303=)
c.1083A>G (p.Val361=)
10g.119676640A>TCA471634931BAG3c.1086A>T (p.Val362=)
c.909A>T (p.Val303=)
c.1083A>T (p.Val361=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676641G>ACA214224874BAG3c.1087G>A (p.Glu363Lys)
c.910G>A (p.Glu304Lys)
c.1084G>A (p.Glu362Lys)
dbSNP gnomAD v4
10g.119676641G>CCA378296611BAG3c.1087G>C (p.Glu363Gln)
c.910G>C (p.Glu304Gln)
c.1084G>C (p.Glu362Gln)
gnomAD v4
10g.119676641G=CA1940196612BAG3c.1087G= (p.Glu363=)
c.910G= (p.Glu304=)
c.1084G= (p.Glu362=)
10g.119676641G>TCA378296610BAG3c.1087G>T (p.Glu363Ter)
c.910G>T (p.Glu304Ter)
c.1084G>T (p.Glu362Ter)
dbSNP
10g.119676642_119677262delCA2573145588BAG3c.1088_1708del (p.Glu363_Pro569del)
c.1085_1705del (p.Glu362_Pro568del)
ClinVar dbSNP
10g.119676642A=CA1940196613BAG3c.1088A= (p.Glu363=)
c.911A= (p.Glu304=)
c.1085A= (p.Glu362=)
10g.119676642A>CCA378296612BAG3c.1088A>C (p.Glu363Ala)
c.911A>C (p.Glu304Ala)
c.1085A>C (p.Glu362Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676642A>GCA378296613BAG3c.1088A>G (p.Glu363Gly)
c.911A>G (p.Glu304Gly)
c.1085A>G (p.Glu362Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676642A>TCA378296614BAG3c.1088A>T (p.Glu363Val)
c.911A>T (p.Glu304Val)
c.1085A>T (p.Glu362Val)
10g.119676643G>ACA5716482BAG3c.1089G>A (p.Glu363=)
c.912G>A (p.Glu304=)
c.1086G>A (p.Glu362=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676643G>CCA378296615BAG3c.1089G>C (p.Glu363Asp)
c.912G>C (p.Glu304Asp)
c.1086G>C (p.Glu362Asp)
gnomAD v4
10g.119676643G=CA1940196614BAG3c.1089G= (p.Glu363=)
c.912G= (p.Glu304=)
c.1086G= (p.Glu362=)
10g.119676643G>TCA378296616BAG3c.1089G>T (p.Glu363Asp)
c.912G>T (p.Glu304Asp)
c.1086G>T (p.Glu362Asp)
10g.119676644G>ACA214224881BAG3c.1090G>A (p.Val364Met)
c.913G>A (p.Val305Met)
c.1087G>A (p.Val363Met)
dbSNP
10g.119676644G>CCA378296617BAG3c.1090G>C (p.Val364Leu)
c.913G>C (p.Val305Leu)
c.1087G>C (p.Val363Leu)
10g.119676644G=CA1940196615BAG3c.1090G= (p.Val364=)
c.913G= (p.Val305=)
c.1087G= (p.Val363=)
10g.119676644G>TCA378296618BAG3c.1090G>T (p.Val364Leu)
c.913G>T (p.Val305Leu)
c.1087G>T (p.Val363Leu)
10g.119676645T>ACA378296619BAG3c.1091T>A (p.Val364Glu)
c.914T>A (p.Val305Glu)
c.1088T>A (p.Val363Glu)
10g.119676645T>CCA378296620BAG3c.1091T>C (p.Val364Ala)
c.914T>C (p.Val305Ala)
c.1088T>C (p.Val363Ala)
10g.119676645T>GCA378296621BAG3c.1091T>G (p.Val364Gly)
c.914T>G (p.Val305Gly)
c.1088T>G (p.Val363Gly)
10g.119676646G>ACA471634937BAG3c.1092G>A (p.Val364=)
c.915G>A (p.Val305=)
c.1089G>A (p.Val363=)
dbSNP gnomAD v2 gnomAD v4
10g.119676646G>CCA471634938BAG3c.1092G>C (p.Val364=)
c.915G>C (p.Val305=)
c.1089G>C (p.Val363=)
10g.119676646G=CA1940196616BAG3c.1092G= (p.Val364=)
c.915G= (p.Val305=)
c.1089G= (p.Val363=)
10g.119676646G>TCA471634939BAG3c.1092G>T (p.Val364=)
c.915G>T (p.Val305=)
c.1089G>T (p.Val363=)
10g.119676647A=CA1940196617BAG3c.1093A= (p.Lys365=)
c.916A= (p.Lys306=)
c.1090A= (p.Lys364=)
10g.119676647A>CCA214224884BAG3c.1093A>C (p.Lys365Gln)
c.916A>C (p.Lys306Gln)
c.1090A>C (p.Lys364Gln)
ClinVar dbSNP gnomAD v4
10g.119676647A>GCA378296623BAG3c.1093A>G (p.Lys365Glu)
c.916A>G (p.Lys306Glu)
c.1090A>G (p.Lys364Glu)
gnomAD v4
10g.119676647A>TCA378296622BAG3c.1093A>T (p.Lys365Ter)
c.916A>T (p.Lys306Ter)
c.1090A>T (p.Lys364Ter)
10g.119676648A>CCA378296626BAG3c.1094A>C (p.Lys365Thr)
c.917A>C (p.Lys306Thr)
c.1091A>C (p.Lys364Thr)
10g.119676648A>GCA378296624BAG3c.1094A>G (p.Lys365Arg)
c.917A>G (p.Lys306Arg)
c.1091A>G (p.Lys364Arg)
10g.119676648A>TCA378296625BAG3c.1094A>T (p.Lys365Ile)
c.917A>T (p.Lys306Ile)
c.1091A>T (p.Lys364Ile)
10g.119676649A>CCA378296627BAG3c.1095A>C (p.Lys365Asn)
c.918A>C (p.Lys306Asn)
c.1092A>C (p.Lys364Asn)
10g.119676649A>GCA471634942BAG3c.1095A>G (p.Lys365=)
c.918A>G (p.Lys306=)
c.1092A>G (p.Lys364=)
10g.119676649A>TCA378296628BAG3c.1095A>T (p.Lys365Asn)
c.918A>T (p.Lys306Asn)
c.1092A>T (p.Lys364Asn)
10g.119676650G>ACA378296629BAG3c.1096G>A (p.Val366Ile)
c.919G>A (p.Val307Ile)
c.1093G>A (p.Val365Ile)
ClinVar dbSNP
10g.119676650G>CCA378296630BAG3c.1096G>C (p.Val366Leu)
c.919G>C (p.Val307Leu)
c.1093G>C (p.Val365Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676650G=CA1940196618BAG3c.1096G= (p.Val366=)
c.919G= (p.Val307=)
c.1093G= (p.Val365=)
10g.119676650G>TCA378296631BAG3c.1096G>T (p.Val366Phe)
c.919G>T (p.Val307Phe)
c.1093G>T (p.Val365Phe)
10g.119676651T>ACA378296632BAG3c.1097T>A (p.Val366Asp)
c.920T>A (p.Val307Asp)
c.1094T>A (p.Val365Asp)
10g.119676651T>CCA378296633BAG3c.1097T>C (p.Val366Ala)
c.920T>C (p.Val307Ala)
c.1094T>C (p.Val365Ala)
10g.119676651T>GCA378296634BAG3c.1097T>G (p.Val366Gly)
c.920T>G (p.Val307Gly)
c.1094T>G (p.Val365Gly)
10g.119676652T>ACA471634950BAG3c.1098T>A (p.Val366=)
c.921T>A (p.Val307=)
c.1095T>A (p.Val365=)
10g.119676652T>CCA471634949BAG3c.1098T>C (p.Val366=)
c.921T>C (p.Val307=)
c.1095T>C (p.Val365=)
10g.119676652T>GCA471634948BAG3c.1098T>G (p.Val366=)
c.921T>G (p.Val307=)
c.1095T>G (p.Val365=)
10g.119676653C>ACA378296635BAG3c.1099C>A (p.Pro367Thr)
c.922C>A (p.Pro308Thr)
c.1096C>A (p.Pro366Thr)
gnomAD v4
10g.119676653C=CA1940196619BAG3c.1099C= (p.Pro367=)
c.922C= (p.Pro308=)
c.1096C= (p.Pro366=)
10g.119676653C>GCA5716483BAG3c.1099C>G (p.Pro367Ala)
c.922C>G (p.Pro308Ala)
c.1096C>G (p.Pro366Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676653C>TCA378296636BAG3c.1099C>T (p.Pro367Ser)
c.922C>T (p.Pro308Ser)
c.1096C>T (p.Pro366Ser)
dbSNP gnomAD v2 gnomAD v4
10g.119676657dupCA645568602BAG3c.1103dup (p.Ala369CysfsTer?)
c.926dup (p.Ala310CysfsTer?)
c.1100dup (p.Ala368CysfsTer?)
COSMIC
10g.119676654C>ACA378296637BAG3c.1100C>A (p.Pro367His)
c.923C>A (p.Pro308His)
c.1097C>A (p.Pro366His)
10g.119676654C=CA1940196620BAG3c.1100C= (p.Pro367=)
c.923C= (p.Pro308=)
c.1097C= (p.Pro366=)
10g.119676654C>GCA237055BAG3c.1100C>G (p.Pro367Arg)
c.923C>G (p.Pro308Arg)
c.1097C>G (p.Pro366Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676654C>TCA214224906BAG3c.1100C>T (p.Pro367Leu)
c.923C>T (p.Pro308Leu)
c.1097C>T (p.Pro366Leu)
ClinVar dbSNP gnomAD v4
10g.119676655C>ACA471634952BAG3c.1101C>A (p.Pro367=)
c.924C>A (p.Pro308=)
c.1098C>A (p.Pro366=)
10g.119676655C=CA1940196621BAG3c.1101C= (p.Pro367=)
c.924C= (p.Pro308=)
c.1098C= (p.Pro366=)
10g.119676655C>GCA471634953BAG3c.1101C>G (p.Pro367=)
c.924C>G (p.Pro308=)
c.1098C>G (p.Pro366=)
10g.119676655C>TCA5716484BAG3c.1101C>T (p.Pro367=)
c.924C>T (p.Pro308=)
c.1098C>T (p.Pro366=)
dbSNP ExAC
10g.119676656C>ACA378296638BAG3c.1102C>A (p.Pro368Thr)
c.925C>A (p.Pro309Thr)
c.1099C>A (p.Pro367Thr)
10g.119676656C>GCA378296639BAG3c.1102C>G (p.Pro368Ala)
c.925C>G (p.Pro309Ala)
c.1099C>G (p.Pro367Ala)
10g.119676656C>TCA378296640BAG3c.1102C>T (p.Pro368Ser)
c.925C>T (p.Pro309Ser)
c.1099C>T (p.Pro367Ser)
10g.119676657C>ACA378296641BAG3c.1103C>A (p.Pro368His)
c.926C>A (p.Pro309His)
c.1100C>A (p.Pro367His)
10g.119676657C=CA1940196622BAG3c.1103C= (p.Pro368=)
c.926C= (p.Pro309=)
c.1100C= (p.Pro367=)
10g.119676657C>GCA378296642BAG3c.1103C>G (p.Pro368Arg)
c.926C>G (p.Pro309Arg)
c.1100C>G (p.Pro367Arg)
gnomAD v4
10g.119676657C>TCA5716485BAG3c.1103C>T (p.Pro368Leu)
c.926C>T (p.Pro309Leu)
c.1100C>T (p.Pro367Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676658T>ACA471634958BAG3c.1104T>A (p.Pro368=)
c.927T>A (p.Pro309=)
c.1101T>A (p.Pro367=)
10g.119676658T>CCA471634959BAG3c.1104T>C (p.Pro368=)
c.927T>C (p.Pro309=)
c.1101T>C (p.Pro367=)
10g.119676658T>GCA471634960BAG3c.1104T>G (p.Pro368=)
c.927T>G (p.Pro309=)
c.1101T>G (p.Pro367=)
10g.119676659G>ACA378296643BAG3c.1105G>A (p.Ala369Thr)
c.928G>A (p.Ala310Thr)
c.1102G>A (p.Ala368Thr)
10g.119676659G>CCA5716486BAG3c.1105G>C (p.Ala369Pro)
c.928G>C (p.Ala310Pro)
c.1102G>C (p.Ala368Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676659G=CA1940196623BAG3c.1105G= (p.Ala369=)
c.928G= (p.Ala310=)
c.1102G= (p.Ala368=)
10g.119676659G>TCA378296644BAG3c.1105G>T (p.Ala369Ser)
c.928G>T (p.Ala310Ser)
c.1102G>T (p.Ala368Ser)
10g.119676660C>ACA378296645BAG3c.1106C>A (p.Ala369Asp)
c.929C>A (p.Ala310Asp)
c.1103C>A (p.Ala368Asp)
10g.119676660C>GCA378296646BAG3c.1106C>G (p.Ala369Gly)
c.929C>G (p.Ala310Gly)
c.1103C>G (p.Ala368Gly)
gnomAD v4
10g.119676660C>TCA378296647BAG3c.1106C>T (p.Ala369Val)
c.929C>T (p.Ala310Val)
c.1103C>T (p.Ala368Val)
ClinVar gnomAD v4
10g.119676661T>ACA471634963BAG3c.1107T>A (p.Ala369=)
c.930T>A (p.Ala310=)
c.1104T>A (p.Ala368=)
dbSNP
10g.119676661T>CCA471634965BAG3c.1107T>C (p.Ala369=)
c.930T>C (p.Ala310=)
c.1104T>C (p.Ala368=)
gnomAD v4
10g.119676661T>GCA471634967BAG3c.1107T>G (p.Ala369=)
c.930T>G (p.Ala310=)
c.1104T>G (p.Ala368=)
10g.119676661T=CA1940196624BAG3c.1107T= (p.Ala369=)
c.930T= (p.Ala310=)
c.1104T= (p.Ala368=)
10g.119676662C>ACA378296650BAG3c.1108C>A (p.Pro370Thr)
c.931C>A (p.Pro311Thr)
c.1105C>A (p.Pro369Thr)
10g.119676662C=CA1940196625BAG3c.1108C= (p.Pro370=)
c.931C= (p.Pro311=)
c.1105C= (p.Pro369=)
10g.119676662C>GCA378296649BAG3c.1108C>G (p.Pro370Ala)
c.931C>G (p.Pro311Ala)
c.1105C>G (p.Pro369Ala)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676662C>TCA378296648BAG3c.1108C>T (p.Pro370Ser)
c.931C>T (p.Pro311Ser)
c.1105C>T (p.Pro369Ser)
10g.119676663C>ACA378296651BAG3c.1109C>A (p.Pro370Gln)
c.932C>A (p.Pro311Gln)
c.1106C>A (p.Pro369Gln)
10g.119676663C=CA1940196626BAG3c.1109C= (p.Pro370=)
c.932C= (p.Pro311=)
c.1106C= (p.Pro369=)
10g.119676663C>GCA378296652BAG3c.1109C>G (p.Pro370Arg)
c.932C>G (p.Pro311Arg)
c.1106C>G (p.Pro369Arg)
10g.119676663C>TCA5716487BAG3c.1109C>T (p.Pro370Leu)
c.932C>T (p.Pro311Leu)
c.1106C>T (p.Pro369Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676664A>CCA471634975BAG3c.1110A>C (p.Pro370=)
c.933A>C (p.Pro311=)
c.1107A>C (p.Pro369=)
10g.119676664A>GCA471634974BAG3c.1110A>G (p.Pro370=)
c.933A>G (p.Pro311=)
c.1107A>G (p.Pro369=)
10g.119676664A>TCA471634972BAG3c.1110A>T (p.Pro370=)
c.933A>T (p.Pro311=)
c.1107A>T (p.Pro369=)
10g.119676665G>ACA378296653BAG3c.1111G>A (p.Val371Ile)
c.934G>A (p.Val312Ile)
c.1108G>A (p.Val370Ile)
10g.119676665G>CCA378296654BAG3c.1111G>C (p.Val371Leu)
c.934G>C (p.Val312Leu)
c.1108G>C (p.Val370Leu)
10g.119676665G>TCA378296655BAG3c.1111G>T (p.Val371Phe)
c.934G>T (p.Val312Phe)
c.1108G>T (p.Val370Phe)
10g.119676666T>ACA378296656BAG3c.1112T>A (p.Val371Asp)
c.935T>A (p.Val312Asp)
c.1109T>A (p.Val370Asp)
10g.119676666T>CCA378296657BAG3c.1112T>C (p.Val371Ala)
c.935T>C (p.Val312Ala)
c.1109T>C (p.Val370Ala)
10g.119676666T>GCA378296658BAG3c.1112T>G (p.Val371Gly)
c.935T>G (p.Val312Gly)
c.1109T>G (p.Val370Gly)
dbSNP gnomAD v3 gnomAD v4
10g.119676666T=CA1940196627BAG3c.1112T= (p.Val371=)
c.935T= (p.Val312=)
c.1109T= (p.Val370=)
10g.119676667T>ACA471634979BAG3c.1113T>A (p.Val371=)
c.936T>A (p.Val312=)
c.1110T>A (p.Val370=)
10g.119676667T>CCA471634981BAG3c.1113T>C (p.Val371=)
c.936T>C (p.Val312=)
c.1110T>C (p.Val370=)
10g.119676667T>GCA471634983BAG3c.1113T>G (p.Val371=)
c.936T>G (p.Val312=)
c.1110T>G (p.Val370=)
10g.119676668C>ACA378296659BAG3c.1114C>A (p.Pro372Thr)
c.937C>A (p.Pro313Thr)
c.1111C>A (p.Pro371Thr)
10g.119676668C=CA1940196628BAG3c.1114C= (p.Pro372=)
c.937C= (p.Pro313=)
c.1111C= (p.Pro371=)
10g.119676668C>GCA378296660BAG3c.1114C>G (p.Pro372Ala)
c.937C>G (p.Pro313Ala)
c.1111C>G (p.Pro371Ala)
dbSNP gnomAD v2 gnomAD v4
10g.119676668C>TCA378296661BAG3c.1114C>T (p.Pro372Ser)
c.937C>T (p.Pro313Ser)
c.1111C>T (p.Pro371Ser)
ClinVar gnomAD v4
10g.119676669delCA2611160294BAG3c.1115del (p.Pro372LeufsTer?)
c.938del (p.Pro313LeufsTer?)
c.1112del (p.Pro371LeufsTer?)
gnomAD v4
10g.119676669C>ACA378296662BAG3c.1115C>A (p.Pro372His)
c.938C>A (p.Pro313His)
c.1112C>A (p.Pro371His)
10g.119676669C=CA1940196629BAG3c.1115C= (p.Pro372=)
c.938C= (p.Pro313=)
c.1112C= (p.Pro371=)
10g.119676669C>GCA378296663BAG3c.1115C>G (p.Pro372Arg)
c.938C>G (p.Pro313Arg)
c.1112C>G (p.Pro371Arg)
10g.119676669C>TCA378296664BAG3c.1115C>T (p.Pro372Leu)
c.938C>T (p.Pro313Leu)
c.1112C>T (p.Pro371Leu)
dbSNP gnomAD v4
10g.119676670T>ACA471634987BAG3c.1116T>A (p.Pro372=)
c.939T>A (p.Pro313=)
c.1113T>A (p.Pro371=)
gnomAD v4
10g.119676670T>CCA471634988BAG3c.1116T>C (p.Pro372=)
c.939T>C (p.Pro313=)
c.1113T>C (p.Pro371=)
10g.119676670T>GCA471634989BAG3c.1116T>G (p.Pro372=)
c.939T>G (p.Pro313=)
c.1113T>G (p.Pro371=)
10g.119676671T>ACA378296667BAG3c.1117T>A (p.Cys373Ser)
c.940T>A (p.Cys314Ser)
c.1114T>A (p.Cys372Ser)
10g.119676671T>CCA378296665BAG3c.1117T>C (p.Cys373Arg)
c.940T>C (p.Cys314Arg)
c.1114T>C (p.Cys372Arg)
ClinVar
10g.119676671T>GCA378296666BAG3c.1117T>G (p.Cys373Gly)
c.940T>G (p.Cys314Gly)
c.1114T>G (p.Cys372Gly)
10g.119676672G>ACA10576780BAG3c.1118G>A (p.Cys373Tyr)
c.941G>A (p.Cys314Tyr)
c.1115G>A (p.Cys372Tyr)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676672G>CCA378296668BAG3c.1118G>C (p.Cys373Ser)
c.941G>C (p.Cys314Ser)
c.1115G>C (p.Cys372Ser)
ClinVar dbSNP
10g.119676672G=CA1940196630BAG3c.1118G= (p.Cys373=)
c.941G= (p.Cys314=)
c.1115G= (p.Cys372=)
10g.119676672G>TCA378296669BAG3c.1118G>T (p.Cys373Phe)
c.941G>T (p.Cys314Phe)
c.1115G>T (p.Cys372Phe)
10g.119676673T>ACA378296670BAG3c.1119T>A (p.Cys373Ter)
c.942T>A (p.Cys314Ter)
c.1116T>A (p.Cys372Ter)
gnomAD v4
10g.119676673T>CCA471634994BAG3c.1119T>C (p.Cys373=)
c.942T>C (p.Cys314=)
c.1116T>C (p.Cys372=)
dbSNP gnomAD v3 gnomAD v4
10g.119676673T>GCA378296671BAG3c.1119T>G (p.Cys373Trp)
c.942T>G (p.Cys314Trp)
c.1116T>G (p.Cys372Trp)
10g.119676673T=CA1940196631BAG3c.1119T= (p.Cys373=)
c.942T= (p.Cys314=)
c.1116T= (p.Cys372=)
10g.119676679_119676681delCA2574694984BAG3c.1125_1127del (p.Pro376del)
c.948_950del (p.Pro317del)
c.1122_1124del (p.Pro375del)
10g.119676674C>ACA378296672BAG3c.1120C>A (p.Pro374Thr)
c.943C>A (p.Pro315Thr)
c.1117C>A (p.Pro373Thr)
10g.119676674C>GCA378296673BAG3c.1120C>G (p.Pro374Ala)
c.943C>G (p.Pro315Ala)
c.1117C>G (p.Pro373Ala)
10g.119676674C>TCA378296674BAG3c.1120C>T (p.Pro374Ser)
c.943C>T (p.Pro315Ser)
c.1117C>T (p.Pro373Ser)
10g.119676675C>ACA378296675BAG3c.1121C>A (p.Pro374His)
c.944C>A (p.Pro315His)
c.1118C>A (p.Pro373His)
10g.119676675C=CA1940196632BAG3c.1121C= (p.Pro374=)
c.944C= (p.Pro315=)
c.1118C= (p.Pro373=)
10g.119676675C>GCA5716488BAG3c.1121C>G (p.Pro374Arg)
c.944C>G (p.Pro315Arg)
c.1118C>G (p.Pro373Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676675C>TCA378296676BAG3c.1121C>T (p.Pro374Leu)
c.944C>T (p.Pro315Leu)
c.1118C>T (p.Pro373Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676676T>ACA471634997BAG3c.1122T>A (p.Pro374=)
c.945T>A (p.Pro315=)
c.1119T>A (p.Pro373=)
10g.119676676T>CCA471634998BAG3c.1122T>C (p.Pro374=)
c.945T>C (p.Pro315=)
c.1119T>C (p.Pro373=)
10g.119676676T>GCA471634999BAG3c.1122T>G (p.Pro374=)
c.945T>G (p.Pro315=)
c.1119T>G (p.Pro373=)
10g.119676677C>ACA378296679BAG3c.1123C>A (p.Pro375Thr)
c.946C>A (p.Pro316Thr)
c.1120C>A (p.Pro374Thr)
10g.119676677C>GCA378296678BAG3c.1123C>G (p.Pro375Ala)
c.946C>G (p.Pro316Ala)
c.1120C>G (p.Pro374Ala)
10g.119676677C>TCA378296677BAG3c.1123C>T (p.Pro375Ser)
c.946C>T (p.Pro316Ser)
c.1120C>T (p.Pro374Ser)
gnomAD v4
10g.119676678C>ACA378296682BAG3c.1124C>A (p.Pro375His)
c.947C>A (p.Pro316His)
c.1121C>A (p.Pro374His)
10g.119676678C>GCA378296680BAG3c.1124C>G (p.Pro375Arg)
c.947C>G (p.Pro316Arg)
c.1121C>G (p.Pro374Arg)
10g.119676678C>TCA378296681BAG3c.1124C>T (p.Pro375Leu)
c.947C>T (p.Pro316Leu)
c.1121C>T (p.Pro374Leu)
COSMIC
10g.119676679T>ACA471635004BAG3c.1125T>A (p.Pro375=)
c.948T>A (p.Pro316=)
c.1122T>A (p.Pro374=)
10g.119676679T>CCA471635005BAG3c.1125T>C (p.Pro375=)
c.948T>C (p.Pro316=)
c.1122T>C (p.Pro374=)
ClinVar dbSNP gnomAD v4
10g.119676679T>GCA471635006BAG3c.1125T>G (p.Pro375=)
c.948T>G (p.Pro316=)
c.1122T>G (p.Pro374=)
10g.119676679T=CA1940196633BAG3c.1125T= (p.Pro375=)
c.948T= (p.Pro316=)
c.1122T= (p.Pro374=)
10g.119676680C>ACA378296683BAG3c.1126C>A (p.Pro376Thr)
c.949C>A (p.Pro317Thr)
c.1123C>A (p.Pro375Thr)
10g.119676680C=CA1940196634BAG3c.1126C= (p.Pro376=)
c.949C= (p.Pro317=)
c.1123C= (p.Pro375=)
10g.119676680C>GCA378296684BAG3c.1126C>G (p.Pro376Ala)
c.949C>G (p.Pro317Ala)
c.1123C>G (p.Pro375Ala)
10g.119676680C>TCA378296685BAG3c.1126C>T (p.Pro376Ser)
c.949C>T (p.Pro317Ser)
c.1123C>T (p.Pro375Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676681C>ACA378296686BAG3c.1127C>A (p.Pro376His)
c.950C>A (p.Pro317His)
c.1124C>A (p.Pro375His)
ClinVar dbSNP gnomAD v4
10g.119676681C>GCA378296687BAG3c.1127C>G (p.Pro376Arg)
c.950C>G (p.Pro317Arg)
c.1124C>G (p.Pro375Arg)
10g.119676681C>TCA378296688BAG3c.1127C>T (p.Pro376Leu)
c.950C>T (p.Pro317Leu)
c.1124C>T (p.Pro375Leu)
dbSNP
10g.119676682C>ACA471635009BAG3c.1128C>A (p.Pro376=)
c.951C>A (p.Pro317=)
c.1125C>A (p.Pro375=)
gnomAD v4
10g.119676682C=CA1940196635BAG3c.1128C= (p.Pro376=)
c.951C= (p.Pro317=)
c.1125C= (p.Pro375=)
10g.119676682C>GCA471635010BAG3c.1128C>G (p.Pro376=)
c.951C>G (p.Pro317=)
c.1125C>G (p.Pro375=)
10g.119676682C>TCA471635011BAG3c.1128C>T (p.Pro376=)
c.951C>T (p.Pro317=)
c.1125C>T (p.Pro375=)
ClinVar dbSNP gnomAD v4
10g.119676683A>CCA378296689BAG3c.1129A>C (p.Ser377Arg)
c.952A>C (p.Ser318Arg)
c.1126A>C (p.Ser376Arg)
10g.119676683A>GCA378296690BAG3c.1129A>G (p.Ser377Gly)
c.952A>G (p.Ser318Gly)
c.1126A>G (p.Ser376Gly)
10g.119676683A>TCA378296691BAG3c.1129A>T (p.Ser377Cys)
c.952A>T (p.Ser318Cys)
c.1126A>T (p.Ser376Cys)
10g.119676684G>ACA378296692BAG3c.1130G>A (p.Ser377Asn)
c.953G>A (p.Ser318Asn)
c.1127G>A (p.Ser376Asn)
10g.119676684G>CCA378296693BAG3c.1130G>C (p.Ser377Thr)
c.953G>C (p.Ser318Thr)
c.1127G>C (p.Ser376Thr)
10g.119676684G>TCA378296694BAG3c.1130G>T (p.Ser377Ile)
c.953G>T (p.Ser318Ile)
c.1127G>T (p.Ser376Ile)
10g.119676685C>ACA378296695BAG3c.1131C>A (p.Ser377Arg)
c.954C>A (p.Ser318Arg)
c.1128C>A (p.Ser376Arg)
10g.119676685C>GCA378296696BAG3c.1131C>G (p.Ser377Arg)
c.954C>G (p.Ser318Arg)
c.1128C>G (p.Ser376Arg)
10g.119676685C>TCA471635014BAG3c.1131C>T (p.Ser377=)
c.954C>T (p.Ser318=)
c.1128C>T (p.Ser376=)
gnomAD v4
10g.119676685_119676688delCA2580616876BAG3c.1131_1134del (p.Ser377ArgfsTer?)
c.954_957del (p.Ser318ArgfsTer?)
c.1128_1131del (p.Ser376ArgfsTer?)
ClinVar
10g.119676686C>ACA378296697BAG3c.1132C>A (p.Pro378Thr)
c.955C>A (p.Pro319Thr)
c.1129C>A (p.Pro377Thr)
10g.119676686C=CA1940196636BAG3c.1132C= (p.Pro378=)
c.955C= (p.Pro319=)
c.1129C= (p.Pro377=)
10g.119676686C>GCA378296698BAG3c.1132C>G (p.Pro378Ala)
c.955C>G (p.Pro319Ala)
c.1129C>G (p.Pro377Ala)
10g.119676686C>TCA5716489BAG3c.1132C>T (p.Pro378Ser)
c.955C>T (p.Pro319Ser)
c.1129C>T (p.Pro377Ser)
dbSNP ExAC gnomAD v2
10g.119676687C>ACA378296699BAG3c.1133C>A (p.Pro378His)
c.956C>A (p.Pro319His)
c.1130C>A (p.Pro377His)
10g.119676687C=CA1940196637BAG3c.1133C= (p.Pro378=)
c.956C= (p.Pro319=)
c.1130C= (p.Pro377=)
10g.119676687C>GCA378296700BAG3c.1133C>G (p.Pro378Arg)
c.956C>G (p.Pro319Arg)
c.1130C>G (p.Pro377Arg)
ClinVar dbSNP
10g.119676687C>TCA378296701BAG3c.1133C>T (p.Pro378Leu)
c.956C>T (p.Pro319Leu)
c.1130C>T (p.Pro377Leu)
dbSNP
10g.119676688T>ACA471635019BAG3c.1134T>A (p.Pro378=)
c.957T>A (p.Pro319=)
c.1131T>A (p.Pro377=)
10g.119676688T>CCA471635020BAG3c.1134T>C (p.Pro378=)
c.957T>C (p.Pro319=)
c.1131T>C (p.Pro377=)
dbSNP
10g.119676688T>GCA471635022BAG3c.1134T>G (p.Pro378=)
c.957T>G (p.Pro319=)
c.1131T>G (p.Pro377=)
10g.119676688T=CA1940196638BAG3c.1134T= (p.Pro378=)
c.957T= (p.Pro319=)
c.1131T= (p.Pro377=)
10g.119676689G>ACA214224945BAG3c.1135G>A (p.Gly379Ser)
c.958G>A (p.Gly320Ser)
c.1132G>A (p.Gly378Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676689G>CCA378296702BAG3c.1135G>C (p.Gly379Arg)
c.958G>C (p.Gly320Arg)
c.1132G>C (p.Gly378Arg)
10g.119676689G=CA1940196639BAG3c.1135G= (p.Gly379=)
c.958G= (p.Gly320=)
c.1132G= (p.Gly378=)
10g.119676689G>TCA378296703BAG3c.1135G>T (p.Gly379Cys)
c.958G>T (p.Gly320Cys)
c.1132G>T (p.Gly378Cys)
10g.119676690delCA1139532245BAG3c.1136del (p.Gly379AlafsTer?)
c.959del (p.Gly320AlafsTer?)
c.1133del (p.Gly378AlafsTer?)
dbSNP
10g.119676690G>ACA378296704BAG3c.1136G>A (p.Gly379Asp)
c.959G>A (p.Gly320Asp)
c.1133G>A (p.Gly378Asp)
10g.119676690G>CCA378296705BAG3c.1136G>C (p.Gly379Ala)
c.959G>C (p.Gly320Ala)
c.1133G>C (p.Gly378Ala)
10g.119676690G>TCA378296706BAG3c.1136G>T (p.Gly379Val)
c.959G>T (p.Gly320Val)
c.1133G>T (p.Gly378Val)
10g.119676691C>ACA471635027BAG3c.1137C>A (p.Gly379=)
c.960C>A (p.Gly320=)
c.1134C>A (p.Gly378=)
10g.119676691C>GCA471635029BAG3c.1137C>G (p.Gly379=)
c.960C>G (p.Gly320=)
c.1134C>G (p.Gly378=)
10g.119676691C>TCA471635031BAG3c.1137C>T (p.Gly379=)
c.960C>T (p.Gly320=)
c.1134C>T (p.Gly378=)
gnomAD v4
10g.119676692C>ACA378296707BAG3c.1138C>A (p.Pro380Thr)
c.961C>A (p.Pro321Thr)
c.1135C>A (p.Pro379Thr)
10g.119676692C=CA1940196640BAG3c.1138C= (p.Pro380=)
c.961C= (p.Pro321=)
c.1135C= (p.Pro379=)
10g.119676692C>GCA378296708BAG3c.1138C>G (p.Pro380Ala)
c.961C>G (p.Pro321Ala)
c.1135C>G (p.Pro379Ala)
10g.119676692C>TCA175304BAG3c.1138C>T (p.Pro380Ser)
c.961C>T (p.Pro321Ser)
c.1135C>T (p.Pro379Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676693C>ACA378296709BAG3c.1139C>A (p.Pro380His)
c.962C>A (p.Pro321His)
c.1136C>A (p.Pro379His)
10g.119676693C=CA1940196641BAG3c.1139C= (p.Pro380=)
c.962C= (p.Pro321=)
c.1136C= (p.Pro379=)
10g.119676693C>GCA378296710BAG3c.1139C>G (p.Pro380Arg)
c.962C>G (p.Pro321Arg)
c.1136C>G (p.Pro379Arg)
gnomAD v4
10g.119676693C>TCA5716490BAG3c.1139C>T (p.Pro380Leu)
c.962C>T (p.Pro321Leu)
c.1136C>T (p.Pro379Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676694T>ACA471635033BAG3c.1140T>A (p.Pro380=)
c.963T>A (p.Pro321=)
c.1137T>A (p.Pro379=)
10g.119676694T>CCA471635035BAG3c.1140T>C (p.Pro380=)
c.963T>C (p.Pro321=)
c.1137T>C (p.Pro379=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676694T>GCA5716491BAG3c.1140T>G (p.Pro380=)
c.963T>G (p.Pro321=)
c.1137T>G (p.Pro379=)
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
10g.119676694T=CA1940196642BAG3c.1140T= (p.Pro380=)
c.963T= (p.Pro321=)
c.1137T= (p.Pro379=)
10g.119676695T>ACA378296711BAG3c.1141T>A (p.Ser381Thr)
c.964T>A (p.Ser322Thr)
c.1138T>A (p.Ser380Thr)
10g.119676695T>CCA5716492BAG3c.1141T>C (p.Ser381Pro)
c.964T>C (p.Ser322Pro)
c.1138T>C (p.Ser380Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676695T>GCA378296712BAG3c.1141T>G (p.Ser381Ala)
c.964T>G (p.Ser322Ala)
c.1138T>G (p.Ser380Ala)
10g.119676695T=CA1940196643BAG3c.1141T= (p.Ser381=)
c.964T= (p.Ser322=)
c.1138T= (p.Ser380=)
10g.119676696C>ACA378296713BAG3c.1142C>A (p.Ser381Tyr)
c.965C>A (p.Ser322Tyr)
c.1139C>A (p.Ser380Tyr)
10g.119676696C=CA1940196644BAG3c.1142C= (p.Ser381=)
c.965C= (p.Ser322=)
c.1139C= (p.Ser380=)
10g.119676696C>GCA5716493BAG3c.1142C>G (p.Ser381Cys)
c.965C>G (p.Ser322Cys)
c.1139C>G (p.Ser380Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676696C>TCA378296714BAG3c.1142C>T (p.Ser381Phe)
c.965C>T (p.Ser322Phe)
c.1139C>T (p.Ser380Phe)
10g.119676697T>ACA471739291BAG3c.1143T>A (p.Ser381=)
c.966T>A (p.Ser322=)
c.1140T>A (p.Ser380=)
10g.119676697T>CCA471739295BAG3c.1143T>C (p.Ser381=)
c.966T>C (p.Ser322=)
c.1140T>C (p.Ser380=)
ClinVar dbSNP
10g.119676697T>GCA471739293BAG3c.1143T>G (p.Ser381=)
c.966T>G (p.Ser322=)
c.1140T>G (p.Ser380=)
10g.119676697T=CA1940196645BAG3c.1143T= (p.Ser381=)
c.966T= (p.Ser322=)
c.1140T= (p.Ser380=)
10g.119676698G>ACA214224952BAG3c.1144G>A (p.Ala382Thr)
c.967G>A (p.Ala323Thr)
c.1141G>A (p.Ala381Thr)
dbSNP gnomAD v4
10g.119676698G>CCA378296715BAG3c.1144G>C (p.Ala382Pro)
c.967G>C (p.Ala323Pro)
c.1141G>C (p.Ala381Pro)
dbSNP gnomAD v2 gnomAD v4
10g.119676698G=CA1940196646BAG3c.1144G= (p.Ala382=)
c.967G= (p.Ala323=)
c.1141G= (p.Ala381=)
10g.119676698G>TCA378296716BAG3c.1144G>T (p.Ala382Ser)
c.967G>T (p.Ala323Ser)
c.1141G>T (p.Ala381Ser)
10g.119676699C>ACA378296717BAG3c.1145C>A (p.Ala382Asp)
c.968C>A (p.Ala323Asp)
c.1142C>A (p.Ala381Asp)
10g.119676699C>GCA378296718BAG3c.1145C>G (p.Ala382Gly)
c.968C>G (p.Ala323Gly)
c.1142C>G (p.Ala381Gly)
10g.119676699C>TCA378296719BAG3c.1145C>T (p.Ala382Val)
c.968C>T (p.Ala323Val)
c.1142C>T (p.Ala381Val)
10g.119676700T>ACA214224956BAG3c.1146T>A (p.Ala382=)
c.969T>A (p.Ala323=)
c.1143T>A (p.Ala381=)
ClinVar dbSNP
10g.119676700T>CCA471739299BAG3c.1146T>C (p.Ala382=)
c.969T>C (p.Ala323=)
c.1143T>C (p.Ala381=)
10g.119676700T>GCA471739300BAG3c.1146T>G (p.Ala382=)
c.969T>G (p.Ala323=)
c.1143T>G (p.Ala381=)
10g.119676700T=CA1940196647BAG3c.1146T= (p.Ala382=)
c.969T= (p.Ala323=)
c.1143T= (p.Ala381=)
10g.119676701G>ACA378296720BAG3c.1147G>A (p.Val383Ile)
c.970G>A (p.Val324Ile)
c.1144G>A (p.Val382Ile)
10g.119676701G>CCA378296722BAG3c.1147G>C (p.Val383Leu)
c.970G>C (p.Val324Leu)
c.1144G>C (p.Val382Leu)
dbSNP
10g.119676701G=CA1940196648BAG3c.1147G= (p.Val383=)
c.970G= (p.Val324=)
c.1144G= (p.Val382=)
10g.119676701G>TCA378296721BAG3c.1147G>T (p.Val383Phe)
c.970G>T (p.Val324Phe)
c.1144G>T (p.Val382Phe)
10g.119676702T>ACA378296723BAG3c.1148T>A (p.Val383Asp)
c.971T>A (p.Val324Asp)
c.1145T>A (p.Val382Asp)
10g.119676702T>CCA378296724BAG3c.1148T>C (p.Val383Ala)
c.971T>C (p.Val324Ala)
c.1145T>C (p.Val382Ala)
ClinVar dbSNP
10g.119676702T>GCA378296725BAG3c.1148T>G (p.Val383Gly)
c.971T>G (p.Val324Gly)
c.1145T>G (p.Val382Gly)
10g.119676702T=CA1940196649BAG3c.1148T= (p.Val383=)
c.971T= (p.Val324=)
c.1145T= (p.Val382=)
10g.119676707_119676714delCA1139532246BAG3c.1153_1160del (p.Ser385GlnfsTer?)
c.1150_1157del (p.Ser384GlnfsTer?)
ClinVar dbSNP
10g.119676703C>ACA471739302BAG3c.1149C>A (p.Val383=)
c.972C>A (p.Val324=)
c.1146C>A (p.Val382=)
dbSNP
10g.119676703C=CA1940196650BAG3c.1149C= (p.Val383=)
c.972C= (p.Val324=)
c.1146C= (p.Val382=)
10g.119676703C>GCA471739303BAG3c.1149C>G (p.Val383=)
c.972C>G (p.Val324=)
c.1146C>G (p.Val382=)
10g.119676703C>TCA5716494BAG3c.1149C>T (p.Val383=)
c.972C>T (p.Val324=)
c.1146C>T (p.Val382=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676704C>ACA378296726BAG3c.1150C>A (p.Pro384Thr)
c.973C>A (p.Pro325Thr)
c.1147C>A (p.Pro383Thr)
dbSNP
10g.119676704C=CA1940196651BAG3c.1150C= (p.Pro384=)
c.973C= (p.Pro325=)
c.1147C= (p.Pro383=)
10g.119676704C>GCA378296727BAG3c.1150C>G (p.Pro384Ala)
c.973C>G (p.Pro325Ala)
c.1147C>G (p.Pro383Ala)
10g.119676704C>TCA378296728BAG3c.1150C>T (p.Pro384Ser)
c.973C>T (p.Pro325Ser)
c.1147C>T (p.Pro383Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676705C>ACA378296729BAG3c.1151C>A (p.Pro384His)
c.974C>A (p.Pro325His)
c.1148C>A (p.Pro383His)
10g.119676705C=CA1940196652BAG3c.1151C= (p.Pro384=)
c.974C= (p.Pro325=)
c.1148C= (p.Pro383=)
10g.119676705C>GCA5716495BAG3c.1151C>G (p.Pro384Arg)
c.974C>G (p.Pro325Arg)
c.1148C>G (p.Pro383Arg)
dbSNP ExAC gnomAD v2
10g.119676705C>TCA5716496BAG3c.1151C>T (p.Pro384Leu)
c.974C>T (p.Pro325Leu)
c.1148C>T (p.Pro383Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676706C>ACA471739308BAG3c.1152C>A (p.Pro384=)
c.975C>A (p.Pro325=)
c.1149C>A (p.Pro383=)
10g.119676706C=CA1940196653BAG3c.1152C= (p.Pro384=)
c.975C= (p.Pro325=)
c.1149C= (p.Pro383=)
10g.119676706C>GCA471739309BAG3c.1152C>G (p.Pro384=)
c.975C>G (p.Pro325=)
c.1149C>G (p.Pro383=)
10g.119676706C>TCA471739306BAG3c.1152C>T (p.Pro384=)
c.975C>T (p.Pro325=)
c.1149C>T (p.Pro383=)
ClinVar dbSNP gnomAD v4
10g.119676708_119676709delCA2611160295BAG3c.1154_1155del (p.Ser385PhefsTer?)
c.1151_1152del (p.Ser384PhefsTer?)
gnomAD v4
10g.119676707T>ACA378296732BAG3c.1153T>A (p.Ser385Thr)
c.976T>A
c.1150T>A (p.Ser384Thr)
10g.119676707T>CCA378296731BAG3c.1153T>C (p.Ser385Pro)
c.976T>C
c.1150T>C (p.Ser384Pro)
10g.119676707T>GCA378296730BAG3c.1153T>G (p.Ser385Ala)
c.976T>G
c.1150T>G (p.Ser384Ala)
10g.119676709_119676711dupCA5716497BAG3c.1155_1157dup (p.Ser386_Pro387insSer)
c.1152_1154dup (p.Ser385_Pro386insSer)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676708C>ACA378296733BAG3c.1154C>A (p.Ser385Tyr)
c.1151C>A (p.Ser384Tyr)
10g.119676708C>GCA378296734BAG3c.1154C>G (p.Ser385Cys)
c.1151C>G (p.Ser384Cys)
10g.119676708C>TCA378296735BAG3c.1154C>T (p.Ser385Phe)
c.1151C>T (p.Ser384Phe)
gnomAD v4
10g.119676709T>ACA471739313BAG3c.1155T>A (p.Ser385=)
c.1152T>A (p.Ser384=)
10g.119676709T>CCA5716498BAG3c.1155T>C (p.Ser385=)
c.1152T>C (p.Ser384=)
ClinVar dbSNP ExAC gnomAD v4
10g.119676709T>GCA471739314BAG3c.1155T>G (p.Ser385=)
c.1152T>G (p.Ser384=)
10g.119676709T=CA1940196654BAG3c.1155T= (p.Ser385=)
c.1152T= (p.Ser384=)
10g.119676710T>ACA378296738BAG3c.1156T>A (p.Ser386Thr)
c.1153T>A (p.Ser385Thr)
10g.119676710T>CCA378296737BAG3c.1156T>C (p.Ser386Pro)
c.1153T>C (p.Ser385Pro)
dbSNP
10g.119676710T>GCA378296736BAG3c.1156T>G (p.Ser386Ala)
c.1153T>G (p.Ser385Ala)
ClinVar dbSNP
10g.119676710T=CA1940196655BAG3c.1156T= (p.Ser386=)
c.1153T= (p.Ser385=)
10g.119676711C>ACA5716499BAG3c.1157C>A (p.Ser386Tyr)
c.1154C>A (p.Ser385Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676711C=CA1940196656BAG3c.1157C= (p.Ser386=)
c.1154C= (p.Ser385=)
10g.119676711C>GCA378296739BAG3c.1157C>G (p.Ser386Cys)
c.1154C>G (p.Ser385Cys)
10g.119676711C>TCA378296740BAG3c.1157C>T (p.Ser386Phe)
c.1154C>T (p.Ser385Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119676715dupCA658656095BAG3c.1161dup (p.Lys388GlnfsTer?)
c.1158dup (p.Lys387GlnfsTer?)
ClinVar dbSNP
10g.119676712C>ACA471739318BAG3c.1158C>A (p.Ser386=)
c.1155C>A (p.Ser385=)
10g.119676712C>GCA471739319BAG3c.1158C>G (p.Ser386=)
c.1155C>G (p.Ser385=)
10g.119676712C>TCA471739320BAG3c.1158C>T (p.Ser386=)
c.1155C>T (p.Ser385=)
10g.119676713C>ACA378296741BAG3c.1159C>A (p.Pro387Thr)
c.1156C>A (p.Pro386Thr)
10g.119676713C=CA1940196657BAG3c.1159C= (p.Pro387=)
c.1156C= (p.Pro386=)
10g.119676713C>GCA378296742BAG3c.1159C>G (p.Pro387Ala)
c.1156C>G (p.Pro386Ala)
10g.119676713C>TCA5716500BAG3c.1159C>T (p.Pro387Ser)
c.1156C>T (p.Pro386Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676714C>ACA378296743BAG3c.1160C>A (p.Pro387His)
c.1157C>A (p.Pro386His)
10g.119676714C=CA1940196658BAG3c.1160C= (p.Pro387=)
c.1157C= (p.Pro386=)
10g.119676714C>GCA378296744BAG3c.1160C>G (p.Pro387Arg)
c.1157C>G (p.Pro386Arg)
10g.119676714C>TCA16612936BAG3c.1160C>T (p.Pro387Leu)
c.1157C>T (p.Pro386Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119676715C>ACA214224968BAG3c.1161C>A (p.Pro387=)
c.1158C>A (p.Pro386=)
ClinVar dbSNP
10g.119676715C=CA1940196659BAG3c.1161C= (p.Pro387=)
c.1158C= (p.Pro386=)
10g.119676715C>GCA471739322BAG3c.1161C>G (p.Pro387=)
c.1158C>G (p.Pro386=)
dbSNP gnomAD v4
10g.119676715C>TCA471739323BAG3c.1161C>T (p.Pro387=)
c.1158C>T (p.Pro386=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676716A=CA1940196660BAG3c.1162A= (p.Lys388=)
c.1159A= (p.Lys387=)
10g.119676716A>CCA378296745BAG3c.1162A>C (p.Lys388Gln)
c.1159A>C (p.Lys387Gln)
10g.119676716A>GCA378296746BAG3c.1162A>G (p.Lys388Glu)
c.1159A>G (p.Lys387Glu)
dbSNP
10g.119676716A>TCA378296747BAG3c.1162A>T (p.Lys388Ter)
c.1159A>T (p.Lys387Ter)
10g.119676717A=CA1940196661BAG3c.1163A= (p.Lys388=)
c.1160A= (p.Lys387=)
10g.119676717A>CCA378296748BAG3c.1163A>C (p.Lys388Thr)
c.1160A>C (p.Lys387Thr)
10g.119676717A>GCA378296749BAG3c.1163A>G (p.Lys388Arg)
c.1160A>G (p.Lys387Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676717A>TCA378296750BAG3c.1163A>T (p.Lys388Met)
c.1160A>T (p.Lys387Met)
10g.119676718G>ACA471739325BAG3c.1164G>A (p.Lys388=)
c.1161G>A (p.Lys387=)
10g.119676718G>CCA378296751BAG3c.1164G>C (p.Lys388Asn)
c.1161G>C (p.Lys387Asn)
10g.119676718G>TCA378296752BAG3c.1164G>T (p.Lys388Asn)
c.1161G>T (p.Lys387Asn)
10g.119676719A=CA1940196662BAG3c.1165A= (p.Ser389=)
c.1162A= (p.Ser388=)
10g.119676719A>CCA378296753BAG3c.1165A>C (p.Ser389Arg)
c.1162A>C (p.Ser388Arg)
10g.119676719A>GCA5716501BAG3c.1165A>G (p.Ser389Gly)
c.1162A>G (p.Ser388Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676719A>TCA378296754BAG3c.1165A>T (p.Ser389Cys)
c.1162A>T (p.Ser388Cys)
10g.119676720G>ACA308218BAG3c.1166G>A (p.Ser389Asn)
c.1163G>A (p.Ser388Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676720G>CCA378296756BAG3c.1166G>C (p.Ser389Thr)
c.1163G>C (p.Ser388Thr)
10g.119676720G=CA1940196663BAG3c.1166G= (p.Ser389=)
c.1163G= (p.Ser388=)
10g.119676720G>TCA378296755BAG3c.1166G>T (p.Ser389Ile)
c.1163G>T (p.Ser388Ile)
10g.119676721T>ACA378296757BAG3c.1167T>A (p.Ser389Arg)
c.1164T>A (p.Ser388Arg)
10g.119676721T>CCA471739327BAG3c.1167T>C (p.Ser389=)
c.1164T>C (p.Ser388=)
dbSNP gnomAD v3 gnomAD v4
10g.119676721T>GCA5716502BAG3c.1167T>G (p.Ser389Arg)
c.1164T>G (p.Ser388Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676721T=CA1940196664BAG3c.1167T= (p.Ser389=)
c.1164T= (p.Ser388=)
10g.119676722G>ACA378296758BAG3c.1168G>A (p.Val390Met)
c.1165G>A (p.Val389Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676722G>CCA378296759BAG3c.1168G>C (p.Val390Leu)
c.1165G>C (p.Val389Leu)
10g.119676722G=CA1940196665BAG3c.1168G= (p.Val390=)
c.1165G= (p.Val389=)
10g.119676722G>TCA378296760BAG3c.1168G>T (p.Val390Leu)
c.1165G>T (p.Val389Leu)
10g.119676723T>ACA378296761BAG3c.1169T>A (p.Val390Glu)
c.1166T>A (p.Val389Glu)
10g.119676723T>CCA378296762BAG3c.1169T>C (p.Val390Ala)
c.1166T>C (p.Val389Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676723T>GCA378296763BAG3c.1169T>G (p.Val390Gly)
c.1166T>G (p.Val389Gly)
ClinVar
10g.119676723T=CA1940196666BAG3c.1169T= (p.Val390=)
c.1166T= (p.Val389=)
10g.119676724G>ACA471739330BAG3c.1170G>A (p.Val390=)
c.1167G>A (p.Val389=)
10g.119676724G>CCA471739332BAG3c.1170G>C (p.Val390=)
c.1167G>C (p.Val389=)
10g.119676724G>TCA471739333BAG3c.1170G>T (p.Val390=)
c.1167G>T (p.Val389=)
10g.119676725G>ACA378296764BAG3c.1171G>A (p.Ala391Thr)
c.1168G>A (p.Ala390Thr)
10g.119676725G>CCA378296765BAG3c.1171G>C (p.Ala391Pro)
c.1168G>C (p.Ala390Pro)
gnomAD v4
10g.119676725G>TCA378296766BAG3c.1171G>T (p.Ala391Ser)
c.1168G>T (p.Ala390Ser)
10g.119676726C>ACA378296767BAG3c.1172C>A (p.Ala391Asp)
c.1169C>A (p.Ala390Asp)
10g.119676726C=CA1940196667BAG3c.1172C= (p.Ala391=)
c.1169C= (p.Ala390=)
10g.119676726C>GCA5716503BAG3c.1172C>G (p.Ala391Gly)
c.1169C>G (p.Ala390Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676726C>TCA237058BAG3c.1172C>T (p.Ala391Val)
c.1169C>T (p.Ala390Val)
ClinVar dbSNP gnomAD v4
10g.119676727T>ACA471739336BAG3c.1173T>A (p.Ala391=)
c.1170T>A (p.Ala390=)
10g.119676727T>CCA471739339BAG3c.1173T>C (p.Ala391=)
c.1170T>C (p.Ala390=)
10g.119676727T>GCA471739338BAG3c.1173T>G (p.Ala391=)
c.1170T>G (p.Ala390=)
ClinVar
10g.119676728A>CCA378296770BAG3c.1174A>C (p.Thr392Pro)
c.1171A>C (p.Thr391Pro)
10g.119676728A>GCA378296769BAG3c.1174A>G (p.Thr392Ala)
c.1171A>G (p.Thr391Ala)
ClinVar dbSNP gnomAD v4
10g.119676728A>TCA378296768BAG3c.1174A>T (p.Thr392Ser)
c.1171A>T (p.Thr391Ser)
10g.119676729C>ACA378296771BAG3c.1175C>A (p.Thr392Lys)
c.1172C>A (p.Thr391Lys)
dbSNP
10g.119676729C=CA1940196668BAG3c.1175C= (p.Thr392=)
c.1172C= (p.Thr391=)
10g.119676729C>GCA378296772BAG3c.1175C>G (p.Thr392Arg)
c.1172C>G (p.Thr391Arg)
10g.119676729C>TCA5716504BAG3c.1175C>T (p.Thr392Ile)
c.1172C>T (p.Thr391Ile)
dbSNP ExAC gnomAD v4
10g.119676729_119676732delinsCAGACA1940196669BAG3c.1175_1178delinsCAGA (p.Thr392=)
c.1172_1175delinsCAGA (p.Thr391=)

Number of alleles fetched