Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119674392_119683124delCA2580082473 ClinVar
10g.119675031_119678711delCA2580082474 ClinVar
10g.119676642_119677262delCA2573145588BAG3c.1088_1708del (p.Glu363_Pro569del)
c.1085_1705del (p.Glu362_Pro568del)
ClinVar dbSNP
10g.119676819_119676829delinsTGCTGAAAGTGCA1940196715BAG3c.1265_1275delinsTGCTGAAAGTG (p.Val422=)
c.1262_1272delinsTGCTGAAAGTG (p.Val421=)
10g.119676821_119676830delCA204624BAG3c.1267_1276del (p.Leu423LysfsTer14)
c.1264_1273del (p.Leu422LysfsTer14)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676826A>CCA378296959BAG3c.1272A>C (p.Lys424Asn)
c.1269A>C (p.Lys423Asn)
10g.119676826A>GCA471739441BAG3c.1272A>G (p.Lys424=)
c.1269A>G (p.Lys423=)
gnomAD v4
10g.119676826A>TCA378296960BAG3c.1272A>T (p.Lys424Asn)
c.1269A>T (p.Lys423Asn)
10g.119676827G>ACA378296961BAG3c.1273G>A (p.Val425Met)
c.1270G>A (p.Val424Met)
10g.119676827G>CCA378296963BAG3c.1273G>C (p.Val425Leu)
c.1270G>C (p.Val424Leu)
10g.119676827G>TCA378296962BAG3c.1273G>T (p.Val425Leu)
c.1270G>T (p.Val424Leu)
10g.119676828T>ACA175313BAG3c.1274T>A (p.Val425Glu)
c.1271T>A (p.Val424Glu)
ClinVar dbSNP gnomAD v4
10g.119676828T>CCA378296964BAG3c.1274T>C (p.Val425Ala)
c.1271T>C (p.Val424Ala)
10g.119676828T>GCA378296965BAG3c.1274T>G (p.Val425Gly)
c.1271T>G (p.Val424Gly)
10g.119676828T=CA1940196718BAG3c.1274T= (p.Val425=)
c.1271T= (p.Val424=)
10g.119676829G>ACA471739446BAG3c.1275G>A (p.Val425=)
c.1272G>A (p.Val424=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676829G>CCA471739447BAG3c.1275G>C (p.Val425=)
c.1272G>C (p.Val424=)
10g.119676829G=CA1940196719BAG3c.1275G= (p.Val425=)
c.1272G= (p.Val424=)
10g.119676829G>TCA471739448BAG3c.1275G>T (p.Val425=)
c.1272G>T (p.Val424=)
10g.119676830delCA2580082437BAG3c.1276del (p.Glu426LysfsTer14)
c.1273del (p.Glu425LysfsTer14)
ClinVar
10g.119676830G>ACA378296966BAG3c.1276G>A (p.Glu426Lys)
c.1273G>A (p.Glu425Lys)
COSMIC
10g.119676830G>CCA378296967BAG3c.1276G>C (p.Glu426Gln)
c.1273G>C (p.Glu425Gln)
10g.119676830G>TCA378296968BAG3c.1276G>T (p.Glu426Ter)
c.1273G>T (p.Glu425Ter)
10g.119676831A>CCA378296969BAG3c.1277A>C (p.Glu426Ala)
c.1274A>C (p.Glu425Ala)
10g.119676831A>GCA378296970BAG3c.1277A>G (p.Glu426Gly)
c.1274A>G (p.Glu425Gly)
10g.119676831A>TCA378296971BAG3c.1277A>T (p.Glu426Val)
c.1274A>T (p.Glu425Val)
10g.119676832A>CCA378296972BAG3c.1278A>C (p.Glu426Asp)
c.1275A>C (p.Glu425Asp)
10g.119676832A>GCA471739451BAG3c.1278A>G (p.Glu426=)
c.1275A>G (p.Glu425=)
10g.119676832A>TCA378296973BAG3c.1278A>T (p.Glu426Asp)
c.1275A>T (p.Glu425Asp)
dbSNP
10g.119676833G>ACA378296976BAG3c.1279G>A (p.Ala427Thr)
c.1276G>A (p.Ala426Thr)
10g.119676833G>CCA378296974BAG3c.1279G>C (p.Ala427Pro)
c.1276G>C (p.Ala426Pro)
gnomAD v4
10g.119676833G>TCA378296975BAG3c.1279G>T (p.Ala427Ser)
c.1276G>T (p.Ala426Ser)
10g.119676834C>ACA378296977BAG3c.1280C>A (p.Ala427Asp)
c.1277C>A (p.Ala426Asp)
10g.119676834C>GCA378296978BAG3c.1280C>G (p.Ala427Gly)
c.1277C>G (p.Ala426Gly)
10g.119676834C>TCA378296979BAG3c.1280C>T (p.Ala427Val)
c.1277C>T (p.Ala426Val)
10g.119676835C>ACA471739453BAG3c.1281C>A (p.Ala427=)
c.1278C>A (p.Ala426=)
10g.119676835C=CA1940196720BAG3c.1281C= (p.Ala427=)
c.1278C= (p.Ala426=)
10g.119676835C>GCA471739454BAG3c.1281C>G (p.Ala427=)
c.1278C>G (p.Ala426=)
10g.119676835C>TCA5716526BAG3c.1281C>T (p.Ala427=)
c.1278C>T (p.Ala426=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676836A>CCA378296980BAG3c.1282A>C (p.Ile428Leu)
c.1279A>C (p.Ile427Leu)
10g.119676836A>GCA378296981BAG3c.1282A>G (p.Ile428Val)
c.1279A>G (p.Ile427Val)
10g.119676836A>TCA378296982BAG3c.1282A>T (p.Ile428Phe)
c.1279A>T (p.Ile427Phe)
10g.119676837T>ACA378296983BAG3c.1283T>A (p.Ile428Asn)
c.1280T>A (p.Ile427Asn)
10g.119676837T>CCA378296984BAG3c.1283T>C (p.Ile428Thr)
c.1280T>C (p.Ile427Thr)
10g.119676837T>GCA378296985BAG3c.1283T>G (p.Ile428Ser)
c.1280T>G (p.Ile427Ser)
10g.119676838C>ACA471739455BAG3c.1284C>A (p.Ile428=)
c.1281C>A (p.Ile427=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676838C=CA1940196721BAG3c.1284C= (p.Ile428=)
c.1281C= (p.Ile427=)
10g.119676838C>GCA378296986BAG3c.1284C>G (p.Ile428Met)
c.1281C>G (p.Ile427Met)
10g.119676838C>TCA471739457BAG3c.1284C>T (p.Ile428=)
c.1281C>T (p.Ile427=)
dbSNP
10g.119676839C>ACA378296987BAG3c.1285C>A (p.Leu429Met)
c.1282C>A (p.Leu428Met)
10g.119676839C=CA1940196722BAG3c.1285C= (p.Leu429=)
c.1282C= (p.Leu428=)
10g.119676839C>GCA378296988BAG3c.1285C>G (p.Leu429Val)
c.1282C>G (p.Leu428Val)
10g.119676839C>TCA5716527BAG3c.1285C>T (p.Leu429=)
c.1282C>T (p.Leu428=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676840T>ACA378296991BAG3c.1286T>A (p.Leu429Gln)
c.1283T>A (p.Leu428Gln)
10g.119676840T>CCA378296989BAG3c.1286T>C (p.Leu429Pro)
c.1283T>C (p.Leu428Pro)
ClinVar dbSNP
10g.119676840T>GCA378296990BAG3c.1286T>G (p.Leu429Arg)
c.1283T>G (p.Leu428Arg)
10g.119676840T=CA1940196723BAG3c.1286T= (p.Leu429=)
c.1283T= (p.Leu428=)
10g.119676841G>ACA471739460BAG3c.1287G>A (p.Leu429=)
c.1284G>A (p.Leu428=)
gnomAD v4
10g.119676841G>CCA471739461BAG3c.1287G>C (p.Leu429=)
c.1284G>C (p.Leu428=)
10g.119676841G>TCA471739463BAG3c.1287G>T (p.Leu429=)
c.1284G>T (p.Leu428=)
10g.119676842G>ACA5716528BAG3c.1288G>A (p.Glu430Lys)
c.1285G>A (p.Glu429Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119676842G>CCA378296992BAG3c.1288G>C (p.Glu430Gln)
c.1285G>C (p.Glu429Gln)
10g.119676842G=CA1940196724BAG3c.1288G= (p.Glu430=)
c.1285G= (p.Glu429=)
10g.119676842G>TCA378296993BAG3c.1288G>T (p.Glu430Ter)
c.1285G>T (p.Glu429Ter)
10g.119676843A=CA1940196725BAG3c.1289A= (p.Glu430=)
c.1286A= (p.Glu429=)
10g.119676843A>CCA378296994BAG3c.1289A>C (p.Glu430Ala)
c.1286A>C (p.Glu429Ala)
10g.119676843A>GCA378296995BAG3c.1289A>G (p.Glu430Gly)
c.1286A>G (p.Glu429Gly)
gnomAD v4
10g.119676843A>TCA5716529BAG3c.1289A>T (p.Glu430Val)
c.1286A>T (p.Glu429Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676844G>ACA471739467BAG3c.1290G>A (p.Glu430=)
c.1287G>A (p.Glu429=)
10g.119676844G>CCA378296996BAG3c.1290G>C (p.Glu430Asp)
c.1287G>C (p.Glu429Asp)
dbSNP gnomAD v3 gnomAD v4
10g.119676844G=CA1940196726BAG3c.1290G= (p.Glu430=)
c.1287G= (p.Glu429=)
10g.119676844G>TCA378296997BAG3c.1290G>T (p.Glu430Asp)
c.1287G>T (p.Glu429Asp)
10g.119676845A=CA1940196727BAG3c.1291A= (p.Lys431=)
c.1288A= (p.Lys430=)
10g.119676845A>CCA378296998BAG3c.1291A>C (p.Lys431Gln)
c.1288A>C (p.Lys430Gln)
10g.119676845A>GCA378296999BAG3c.1291A>G (p.Lys431Glu)
c.1288A>G (p.Lys430Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676845A>TCA378297000BAG3c.1291A>T (p.Lys431Ter)
c.1288A>T (p.Lys430Ter)
10g.119676846dupCA10587696BAG3c.1292dup (p.Val432GlyfsTer12)
c.1289dup (p.Val431GlyfsTer12)
ClinVar dbSNP gnomAD v4
10g.119676846A>CCA378297003BAG3c.1292A>C (p.Lys431Thr)
c.1289A>C (p.Lys430Thr)
10g.119676846A>GCA378297001BAG3c.1292A>G (p.Lys431Arg)
c.1289A>G (p.Lys430Arg)
10g.119676846A>TCA378297002BAG3c.1292A>T (p.Lys431Met)
c.1289A>T (p.Lys430Met)
10g.119676847G>ACA471739469BAG3c.1293G>A (p.Lys431=)
c.1290G>A (p.Lys430=)
dbSNP
10g.119676847G>CCA378297004BAG3c.1293G>C (p.Lys431Asn)
c.1290G>C (p.Lys430Asn)
ClinVar
10g.119676847G=CA1940196728BAG3c.1293G= (p.Lys431=)
c.1290G= (p.Lys430=)
10g.119676847G>TCA378297005BAG3c.1293G>T (p.Lys431Asn)
c.1290G>T (p.Lys430Asn)
10g.119676848G>ACA378297006BAG3c.1294G>A (p.Val432Ile)
c.1291G>A (p.Val431Ile)
dbSNP gnomAD v3 gnomAD v4
10g.119676848G>CCA378297007BAG3c.1294G>C (p.Val432Leu)
c.1291G>C (p.Val431Leu)
10g.119676848G=CA1940196729BAG3c.1294G= (p.Val432=)
c.1291G= (p.Val431=)
10g.119676848G>TCA378297008BAG3c.1294G>T (p.Val432Leu)
c.1291G>T (p.Val431Leu)
gnomAD v4
10g.119676849T>ACA378297009BAG3c.1295T>A (p.Val432Glu)
c.1292T>A (p.Val431Glu)
10g.119676849T>CCA378297010BAG3c.1295T>C (p.Val432Ala)
c.1292T>C (p.Val431Ala)
10g.119676849T>GCA378297011BAG3c.1295T>G (p.Val432Gly)
c.1292T>G (p.Val431Gly)
10g.119676850A=CA1940196730BAG3c.1296A= (p.Val432=)
c.1293A= (p.Val431=)
10g.119676850A>CCA471739473BAG3c.1296A>C (p.Val432=)
c.1293A>C (p.Val431=)
10g.119676850A>GCA282458BAG3c.1296A>G (p.Val432=)
c.1293A>G (p.Val431=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676850A>TCA471739474BAG3c.1296A>T (p.Val432=)
c.1293A>T (p.Val431=)
10g.119676850_119676851delinsGTCA658656099BAG3c.1296_1297delinsGT (p.Val433Ter)
c.1293_1294delinsGT (p.Val432Ter)
ClinVar
10g.119676850_119676852delinsGCGCA2580082438BAG3c.1296_1298delinsGCG (p.Gln433Arg)
c.1293_1295delinsGCG (p.Gln432Arg)
ClinVar
10g.119676851C>ACA378297012BAG3c.1297C>A (p.Gln433Lys)
c.1294C>A (p.Gln432Lys)
10g.119676851C=CA1940196731BAG3c.1297C= (p.Gln433=)
c.1294C= (p.Gln432=)
10g.119676851C>GCA378297013BAG3c.1297C>G (p.Gln433Glu)
c.1294C>G (p.Gln432Glu)
10g.119676851C>TCA346200BAG3c.1297C>T (p.Gln433Ter)
c.1294C>T (p.Gln432Ter)
ClinVar dbSNP
10g.119676852A=CA1940196732BAG3c.1298A= (p.Gln433=)
c.1295A= (p.Gln432=)
10g.119676852A>CCA378297015BAG3c.1298A>C (p.Gln433Pro)
c.1295A>C (p.Gln432Pro)
10g.119676852A>GCA10634766BAG3c.1298A>G (p.Gln433Arg)
c.1295A>G (p.Gln432Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676852A>TCA378297014BAG3c.1298A>T (p.Gln433Leu)
c.1295A>T (p.Gln432Leu)
10g.119676853G>ACA214225130BAG3c.1299G>A (p.Gln433=)
c.1296G>A (p.Gln432=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676853G>CCA378297016BAG3c.1299G>C (p.Gln433His)
c.1296G>C (p.Gln432His)
10g.119676853G=CA1940196733BAG3c.1299G= (p.Gln433=)
c.1296G= (p.Gln432=)
10g.119676853G>TCA378297017BAG3c.1299G>T (p.Gln433His)
c.1296G>T (p.Gln432His)
10g.119676854G>ACA378297018BAG3c.1300G>A (p.Gly434Arg)
c.1297G>A (p.Gly433Arg)
dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.119676854G>CCA378297019BAG3c.1300G>C (p.Gly434Arg)
c.1297G>C (p.Gly433Arg)
10g.119676854G=CA1940196734BAG3c.1300G= (p.Gly434=)
c.1297G= (p.Gly433=)
10g.119676854G>TCA378297020BAG3c.1300G>T (p.Gly434Trp)
c.1297G>T (p.Gly433Trp)
10g.119676854_119676863dupCA1139532248BAG3c.1300_1309dup (p.Gln437ArgfsTer10)
c.1297_1306dup (p.Gln436ArgfsTer10)
dbSNP
10g.119676855G>ACA378297021BAG3c.1301G>A (p.Gly434Glu)
c.1298G>A (p.Gly433Glu)
gnomAD v4
10g.119676855G>CCA378297022BAG3c.1301G>C (p.Gly434Ala)
c.1298G>C (p.Gly433Ala)
10g.119676855G>TCA378297023BAG3c.1301G>T (p.Gly434Val)
c.1298G>T (p.Gly433Val)
10g.119676856G>ACA471739479BAG3c.1302G>A (p.Gly434=)
c.1299G>A (p.Gly433=)
ClinVar dbSNP gnomAD v4
10g.119676856G>CCA471739480BAG3c.1302G>C (p.Gly434=)
c.1299G>C (p.Gly433=)
10g.119676856G=CA1940196735BAG3c.1302G= (p.Gly434=)
c.1299G= (p.Gly433=)
10g.119676856G>TCA471739481BAG3c.1302G>T (p.Gly434=)
c.1299G>T (p.Gly433=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676857C>ACA378297024BAG3c.1303C>A (p.Leu435Met)
c.1300C>A (p.Leu434Met)
gnomAD v4
10g.119676857C=CA1940196736BAG3c.1303C= (p.Leu435=)
c.1300C= (p.Leu434=)
10g.119676857C>GCA378297025BAG3c.1303C>G (p.Leu435Val)
c.1300C>G (p.Leu434Val)
10g.119676857C>TCA5716530BAG3c.1303C>T (p.Leu435=)
c.1300C>T (p.Leu434=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676858T>ACA378297027BAG3c.1304T>A (p.Leu435Gln)
c.1301T>A (p.Leu434Gln)
10g.119676858T>CCA378297028BAG3c.1304T>C (p.Leu435Pro)
c.1301T>C (p.Leu434Pro)
10g.119676858T>GCA378297026BAG3c.1304T>G (p.Leu435Arg)
c.1301T>G (p.Leu434Arg)
10g.119676859G>ACA471739483BAG3c.1305G>A (p.Leu435=)
c.1302G>A (p.Leu434=)
10g.119676859G>CCA471739485BAG3c.1305G>C (p.Leu435=)
c.1302G>C (p.Leu434=)
10g.119676859G>TCA471739486BAG3c.1305G>T (p.Leu435=)
c.1302G>T (p.Leu434=)
COSMIC
10g.119676860G>ACA378297029BAG3c.1306G>A (p.Glu436Lys)
c.1303G>A (p.Glu435Lys)
10g.119676860G>CCA378297030BAG3c.1306G>C (p.Glu436Gln)
c.1303G>C (p.Glu435Gln)
10g.119676860G>TCA378297031BAG3c.1306G>T (p.Glu436Ter)
c.1303G>T (p.Glu435Ter)
ClinVar
10g.119676861A=CA1940196737BAG3c.1307A= (p.Glu436=)
c.1304A= (p.Glu435=)
10g.119676861A>CCA378297032BAG3c.1307A>C (p.Glu436Ala)
c.1304A>C (p.Glu435Ala)
10g.119676861A>GCA378297033BAG3c.1307A>G (p.Glu436Gly)
c.1304A>G (p.Glu435Gly)
ClinVar dbSNP
10g.119676861A>TCA378297034BAG3c.1307A>T (p.Glu436Val)
c.1304A>T (p.Glu435Val)
10g.119676862G>ACA471739487BAG3c.1308G>A (p.Glu436=)
c.1305G>A (p.Glu435=)
gnomAD v4
10g.119676862G>CCA378297035BAG3c.1308G>C (p.Glu436Asp)
c.1305G>C (p.Glu435Asp)
10g.119676862G>TCA378297036BAG3c.1308G>T (p.Glu436Asp)
c.1305G>T (p.Glu435Asp)
10g.119676863C>ACA378297037BAG3c.1309C>A (p.Gln437Lys)
c.1306C>A (p.Gln436Lys)
gnomAD v4
10g.119676863C>GCA378297038BAG3c.1309C>G (p.Gln437Glu)
c.1306C>G (p.Gln436Glu)
10g.119676863C>TCA378297039BAG3c.1309C>T (p.Gln437Ter)
c.1306C>T (p.Gln436Ter)
10g.119676864A>CCA378297040BAG3c.1310A>C (p.Gln437Pro)
c.1307A>C (p.Gln436Pro)
10g.119676864A>GCA378297042BAG3c.1310A>G (p.Gln437Arg)
c.1307A>G (p.Gln436Arg)
10g.119676864A>TCA378297043BAG3c.1310A>T (p.Gln437Leu)
c.1307A>T (p.Gln436Leu)
10g.119676865G>ACA471739489BAG3c.1311G>A (p.Gln437=)
c.1308G>A (p.Gln436=)
10g.119676865G>CCA378297045BAG3c.1311G>C (p.Gln437His)
c.1308G>C (p.Gln436His)
10g.119676865G>TCA378297044BAG3c.1311G>T (p.Gln437His)
c.1308G>T (p.Gln436His)
10g.119676866G>ACA378297046BAG3c.1312G>A (p.Ala438Thr)
c.1309G>A (p.Ala437Thr)
10g.119676866G>CCA378297047BAG3c.1312G>C (p.Ala438Pro)
c.1309G>C (p.Ala437Pro)
10g.119676866G=CA1940196738BAG3c.1312G= (p.Ala438=)
c.1309G= (p.Ala437=)
10g.119676866G>TCA214225133BAG3c.1312G>T (p.Ala438Ser)
c.1309G>T (p.Ala437Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676867C>ACA378297048BAG3c.1313C>A (p.Ala438Asp)
c.1310C>A (p.Ala437Asp)
10g.119676867C=CA1940196739BAG3c.1313C= (p.Ala438=)
c.1310C= (p.Ala437=)
10g.119676867C>GCA378297050BAG3c.1313C>G (p.Ala438Gly)
c.1310C>G (p.Ala437Gly)
10g.119676867C>TCA378297049BAG3c.1313C>T (p.Ala438Val)
c.1310C>T (p.Ala437Val)
dbSNP gnomAD v2 gnomAD v4
10g.119676868T>ACA471739491BAG3c.1314T>A (p.Ala438=)
c.1311T>A (p.Ala437=)
10g.119676868T>CCA471739492BAG3c.1314T>C (p.Ala438=)
c.1311T>C (p.Ala437=)
ClinVar dbSNP gnomAD v4
10g.119676868T>GCA471739493BAG3c.1314T>G (p.Ala438=)
c.1311T>G (p.Ala437=)
gnomAD v4
10g.119676868T=CA1940196740BAG3c.1314T= (p.Ala438=)
c.1311T= (p.Ala437=)
10g.119676869G>ACA378297051BAG3c.1315G>A (p.Val439Ile)
c.1312G>A (p.Val438Ile)
gnomAD v4
10g.119676869G>CCA378297053BAG3c.1315G>C (p.Val439Leu)
c.1312G>C (p.Val438Leu)
10g.119676869G>TCA378297052BAG3c.1315G>T (p.Val439Leu)
c.1312G>T (p.Val438Leu)
10g.119676870T>ACA378297054BAG3c.1316T>A (p.Val439Glu)
c.1313T>A (p.Val438Glu)
10g.119676870T>CCA378297055BAG3c.1316T>C (p.Val439Ala)
c.1313T>C (p.Val438Ala)
dbSNP gnomAD v3 gnomAD v4
10g.119676870T>GCA378297056BAG3c.1316T>G (p.Val439Gly)
c.1313T>G (p.Val438Gly)
10g.119676870T=CA1940196741BAG3c.1316T= (p.Val439=)
c.1313T= (p.Val438=)
10g.119676870_119676871delCA1139532249BAG3c.1316_1317del (p.Val439GlyfsTer4)
c.1313_1314del (p.Val438GlyfsTer4)
dbSNP
10g.119676871A>CCA471739498BAG3c.1317A>C (p.Val439=)
c.1314A>C (p.Val438=)
10g.119676871A>GCA471739499BAG3c.1317A>G (p.Val439=)
c.1314A>G (p.Val438=)
10g.119676871A>TCA471739500BAG3c.1317A>T (p.Val439=)
c.1314A>T (p.Val438=)
10g.119676872G>ACA10582710BAG3c.1318G>A (p.Asp440Asn)
c.1315G>A (p.Asp439Asn)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676872G>CCA378297057BAG3c.1318G>C (p.Asp440His)
c.1315G>C (p.Asp439His)
10g.119676872G=CA1940196742BAG3c.1318G= (p.Asp440=)
c.1315G= (p.Asp439=)
10g.119676872G>TCA378297058BAG3c.1318G>T (p.Asp440Tyr)
c.1315G>T (p.Asp439Tyr)
10g.119676873A=CA1940196743BAG3c.1319A= (p.Asp440=)
c.1316A= (p.Asp439=)
10g.119676873A>CCA5716531BAG3c.1319A>C (p.Asp440Ala)
c.1316A>C (p.Asp439Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676873A>GCA378297059BAG3c.1319A>G (p.Asp440Gly)
c.1316A>G (p.Asp439Gly)
COSMIC
10g.119676873A>TCA378297060BAG3c.1319A>T (p.Asp440Val)
c.1316A>T (p.Asp439Val)
10g.119676874C>ACA378297061BAG3c.1320C>A (p.Asp440Glu)
c.1317C>A (p.Asp439Glu)
10g.119676874C>GCA378297062BAG3c.1320C>G (p.Asp440Glu)
c.1317C>G (p.Asp439Glu)
10g.119676874C>TCA471739501BAG3c.1320C>T (p.Asp440=)
c.1317C>T (p.Asp439=)
10g.119676875A=CA1940196744BAG3c.1321A= (p.Asn441=)
c.1318A= (p.Asn440=)
10g.119676875A>CCA378297063BAG3c.1321A>C (p.Asn441His)
c.1318A>C (p.Asn440His)
10g.119676875A>GCA237061BAG3c.1321A>G (p.Asn441Asp)
c.1318A>G (p.Asn440Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676875A>TCA378297064BAG3c.1321A>T (p.Asn441Tyr)
c.1318A>T (p.Asn440Tyr)
10g.119676876A>CCA378297065BAG3c.1322A>C (p.Asn441Thr)
c.1319A>C (p.Asn440Thr)
gnomAD v4
10g.119676876A>GCA378297066BAG3c.1322A>G (p.Asn441Ser)
c.1319A>G (p.Asn440Ser)
10g.119676876A>TCA378297067BAG3c.1322A>T (p.Asn441Ile)
c.1319A>T (p.Asn440Ile)
gnomAD v4
10g.119676877C>ACA378297068BAG3c.1323C>A (p.Asn441Lys)
c.1320C>A (p.Asn440Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676877C=CA1940196745BAG3c.1323C= (p.Asn441=)
c.1320C= (p.Asn440=)
10g.119676877C>GCA378297069BAG3c.1323C>G (p.Asn441Lys)
c.1320C>G (p.Asn440Lys)
ClinVar dbSNP
10g.119676877C>TCA471739503BAG3c.1323C>T (p.Asn441=)
c.1320C>T (p.Asn440=)
gnomAD v4
10g.119676878T>ACA378297070BAG3c.1324T>A (p.Phe442Ile)
c.1321T>A (p.Phe441Ile)
10g.119676878T>CCA378297071BAG3c.1324T>C (p.Phe442Leu)
c.1321T>C (p.Phe441Leu)
10g.119676878T>GCA378297072BAG3c.1324T>G (p.Phe442Val)
c.1321T>G (p.Phe441Val)
10g.119676880dupCA2573145590BAG3c.1326dup (p.Glu443Ter)
c.1323dup (p.Glu442Ter)
ClinVar dbSNP
10g.119676879T>ACA378297073BAG3c.1325T>A (p.Phe442Tyr)
c.1322T>A (p.Phe441Tyr)
10g.119676879T>CCA378297074BAG3c.1325T>C (p.Phe442Ser)
c.1322T>C (p.Phe441Ser)
10g.119676879T>GCA214225159BAG3c.1325T>G (p.Phe442Cys)
c.1322T>G (p.Phe441Cys)
dbSNP
10g.119676879T=CA1940196746BAG3c.1325T= (p.Phe442=)
c.1322T= (p.Phe441=)
10g.119676880T>ACA378297075BAG3c.1326T>A (p.Phe442Leu)
c.1323T>A (p.Phe441Leu)
10g.119676880T>CCA471739505BAG3c.1326T>C (p.Phe442=)
c.1323T>C (p.Phe441=)
10g.119676880T>GCA378297076BAG3c.1326T>G (p.Phe442Leu)
c.1323T>G (p.Phe441Leu)
10g.119676881G>ACA378297077BAG3c.1327G>A (p.Glu443Lys)
c.1324G>A (p.Glu442Lys)
ClinVar gnomAD v4
10g.119676881G>CCA378297078BAG3c.1327G>C (p.Glu443Gln)
c.1324G>C (p.Glu442Gln)
10g.119676881G>TCA378297079BAG3c.1327G>T (p.Glu443Ter)
c.1324G>T (p.Glu442Ter)
10g.119676882A=CA1940196747BAG3c.1328A= (p.Glu443=)
c.1325A= (p.Glu442=)
10g.119676882A>CCA378297081BAG3c.1328A>C (p.Glu443Ala)
c.1325A>C (p.Glu442Ala)
10g.119676882A>GCA214225163BAG3c.1328A>G (p.Glu443Gly)
c.1325A>G (p.Glu442Gly)
dbSNP
10g.119676882A>TCA378297080BAG3c.1328A>T (p.Glu443Val)
c.1325A>T (p.Glu442Val)
10g.119676883A=CA1940196748BAG3c.1329A= (p.Glu443=)
c.1326A= (p.Glu442=)
10g.119676883A>CCA378297082BAG3c.1329A>C (p.Glu443Asp)
c.1326A>C (p.Glu442Asp)
10g.119676883A>GCA471739509BAG3c.1329A>G (p.Glu443=)
c.1326A>G (p.Glu442=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676883A>TCA378297083BAG3c.1329A>T (p.Glu443Asp)
c.1326A>T (p.Glu442Asp)
10g.119676883_119676884insAGTTCA2789707793BAG3c.1329_1330insAGTT (p.Gly444SerfsTer6)
c.1326_1327insAGTT (p.Gly443SerfsTer6)
10g.119676884G>ACA378297084BAG3c.1330G>A (p.Gly444Ser)
c.1327G>A (p.Gly443Ser)
10g.119676884G>CCA378297085BAG3c.1330G>C (p.Gly444Arg)
c.1327G>C (p.Gly443Arg)
10g.119676884G>TCA378297086BAG3c.1330G>T (p.Gly444Cys)
c.1327G>T (p.Gly443Cys)
10g.119676885G>ACA378297087BAG3c.1331G>A (p.Gly444Asp)
c.1328G>A (p.Gly443Asp)
ClinVar
10g.119676885G>CCA378297089BAG3c.1331G>C (p.Gly444Ala)
c.1328G>C (p.Gly443Ala)
10g.119676885G>TCA378297088BAG3c.1331G>T (p.Gly444Val)
c.1328G>T (p.Gly443Val)
10g.119676885_119676886insACCAGAACTCCCTCCTGGACACATCCCAATTCA2789707794BAG3c.1331_1332insACCAGAACTCCCTCCTGGACACATCCCAATT (p.Lys445ProfsTer14)
c.1328_1329insACCAGAACTCCCTCCTGGACACATCCCAATT (p.Lys444ProfsTer14)
10g.119676886C>ACA471739512BAG3c.1332C>A (p.Gly444=)
c.1329C>A (p.Gly443=)
10g.119676886C>GCA471739513BAG3c.1332C>G (p.Gly444=)
c.1329C>G (p.Gly443=)
10g.119676886C>TCA471739514BAG3c.1332C>T (p.Gly444=)
c.1329C>T (p.Gly443=)
10g.119676887A>CCA378297090BAG3c.1333A>C (p.Lys445Gln)
c.1330A>C (p.Lys444Gln)
10g.119676887A>GCA378297091BAG3c.1333A>G (p.Lys445Glu)
c.1330A>G (p.Lys444Glu)
10g.119676887A>TCA378297092BAG3c.1333A>T (p.Lys445Ter)
c.1330A>T (p.Lys444Ter)
10g.119676888A>CCA378297093BAG3c.1334A>C (p.Lys445Thr)
c.1331A>C (p.Lys444Thr)
10g.119676888A>GCA378297094BAG3c.1334A>G (p.Lys445Arg)
c.1331A>G (p.Lys444Arg)
ClinVar
10g.119676888A>TCA378297095BAG3c.1334A>T (p.Lys445Met)
c.1331A>T (p.Lys444Met)
10g.119676889G>ACA471739516BAG3c.1335G>A (p.Lys445=)
c.1332G>A (p.Lys444=)
10g.119676889G>CCA378297096BAG3c.1335G>C (p.Lys445Asn)
c.1332G>C (p.Lys444Asn)
10g.119676889G>TCA378297097BAG3c.1335G>T (p.Lys445Asn)
c.1332G>T (p.Lys444Asn)
10g.119676890A>CCA378297098BAG3c.1336A>C (p.Lys446Gln)
c.1333A>C (p.Lys445Gln)
10g.119676890A>GCA378297099BAG3c.1336A>G (p.Lys446Glu)
c.1333A>G (p.Lys445Glu)
10g.119676890A>TCA378297100BAG3c.1336A>T (p.Lys446Ter)
c.1333A>T (p.Lys445Ter)
10g.119676891A=CA1940196749BAG3c.1337A= (p.Lys446=)
c.1334A= (p.Lys445=)
10g.119676891A>CCA378297102BAG3c.1337A>C (p.Lys446Thr)
c.1334A>C (p.Lys445Thr)
10g.119676891A>GCA5716532BAG3c.1337A>G (p.Lys446Arg)
c.1334A>G (p.Lys445Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676891A>TCA378297101BAG3c.1337A>T (p.Lys446Met)
c.1334A>T (p.Lys445Met)
10g.119676892G>ACA5716533BAG3c.1338G>A (p.Lys446=)
c.1335G>A (p.Lys445=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676892G>CCA378297103BAG3c.1338G>C (p.Lys446Asn)
c.1335G>C (p.Lys445Asn)
10g.119676892G=CA1940196750BAG3c.1338G= (p.Lys446=)
c.1335G= (p.Lys445=)
10g.119676892G>TCA378297104BAG3c.1338G>T (p.Lys446Asn)
c.1335G>T (p.Lys445Asn)
10g.119676893A>CCA378297105BAG3c.1339A>C (p.Thr447Pro)
c.1336A>C (p.Thr446Pro)
10g.119676893A>GCA378297106BAG3c.1339A>G (p.Thr447Ala)
c.1336A>G (p.Thr446Ala)
10g.119676893A>TCA378297107BAG3c.1339A>T (p.Thr447Ser)
c.1336A>T (p.Thr446Ser)
10g.119676894C>ACA378297108BAG3c.1340C>A (p.Thr447Asn)
c.1337C>A (p.Thr446Asn)
dbSNP gnomAD v2 gnomAD v4
10g.119676894C=CA1940196751BAG3c.1340C= (p.Thr447=)
c.1337C= (p.Thr446=)
10g.119676894C>GCA378297109BAG3c.1340C>G (p.Thr447Ser)
c.1337C>G (p.Thr446Ser)
10g.119676894C>TCA378297110BAG3c.1340C>T (p.Thr447Ile)
c.1337C>T (p.Thr446Ile)
10g.119676895T>ACA471739521BAG3c.1341T>A (p.Thr447=)
c.1338T>A (p.Thr446=)
10g.119676895T>CCA471739522BAG3c.1341T>C (p.Thr447=)
c.1338T>C (p.Thr446=)
gnomAD v4
10g.119676895T>GCA471739523BAG3c.1341T>G (p.Thr447=)
c.1338T>G (p.Thr446=)
10g.119676896G>ACA378297111BAG3c.1342G>A (p.Asp448Asn)
c.1339G>A (p.Asp447Asn)
dbSNP gnomAD v3 gnomAD v4
10g.119676896G>CCA378297112BAG3c.1342G>C (p.Asp448His)
c.1339G>C (p.Asp447His)
10g.119676896G=CA1940196752BAG3c.1342G= (p.Asp448=)
c.1339G= (p.Asp447=)
10g.119676896G>TCA378297113BAG3c.1342G>T (p.Asp448Tyr)
c.1339G>T (p.Asp447Tyr)
10g.119676897A>CCA378297116BAG3c.1343A>C (p.Asp448Ala)
c.1340A>C (p.Asp447Ala)
10g.119676897A>GCA378297115BAG3c.1343A>G (p.Asp448Gly)
c.1340A>G (p.Asp447Gly)
10g.119676897A>TCA378297114BAG3c.1343A>T (p.Asp448Val)
c.1340A>T (p.Asp447Val)
10g.119676898delCA2499220176BAG3c.1344del (p.Asp448GlufsTer5)
c.1341del (p.Asp447GlufsTer5)
dbSNP
10g.119676898C>ACA378297117BAG3c.1344C>A (p.Asp448Glu)
c.1341C>A (p.Asp447Glu)
10g.119676898C=CA1940196753BAG3c.1344C= (p.Asp448=)
c.1341C= (p.Asp447=)
10g.119676898C>GCA378297118BAG3c.1344C>G (p.Asp448Glu)
c.1341C>G (p.Asp447Glu)
10g.119676898C>TCA184220BAG3c.1344C>T (p.Asp448=)
c.1341C>T (p.Asp447=)
ClinVar dbSNP gnomAD v4
10g.119676899A=CA1940196754BAG3c.1345A= (p.Lys449=)
c.1342A= (p.Lys448=)
10g.119676899A>CCA378297119BAG3c.1345A>C (p.Lys449Gln)
c.1342A>C (p.Lys448Gln)
10g.119676899A>GCA378297120BAG3c.1345A>G (p.Lys449Glu)
c.1342A>G (p.Lys448Glu)
dbSNP gnomAD v2 gnomAD v4
10g.119676899A>TCA16612754BAG3c.1345A>T (p.Lys449Ter)
c.1342A>T (p.Lys448Ter)
ClinVar dbSNP
10g.119676900A>CCA378297121BAG3c.1346A>C (p.Lys449Thr)
c.1343A>C (p.Lys448Thr)
10g.119676900A>GCA378297122BAG3c.1346A>G (p.Lys449Arg)
c.1343A>G (p.Lys448Arg)
gnomAD v4
10g.119676900A>TCA378297123BAG3c.1346A>T (p.Lys449Ile)
c.1343A>T (p.Lys448Ile)
10g.119676901A>CCA378297124BAG3c.1347A>C (p.Lys449Asn)
c.1344A>C (p.Lys448Asn)
10g.119676901A>GCA471739528BAG3c.1347A>G (p.Lys449=)
c.1344A>G (p.Lys448=)
10g.119676901A>TCA378297125BAG3c.1347A>T (p.Lys449Asn)
c.1344A>T (p.Lys448Asn)
10g.119676902A=CA1940196755BAG3c.1348A= (p.Lys450=)
c.1345A= (p.Lys449=)
10g.119676902A>CCA378297126BAG3c.1348A>C (p.Lys450Gln)
c.1345A>C (p.Lys449Gln)
10g.119676902A>GCA5716534BAG3c.1348A>G (p.Lys450Glu)
c.1345A>G (p.Lys449Glu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676902A>TCA378297127BAG3c.1348A>T (p.Lys450Ter)
c.1345A>T (p.Lys449Ter)
ClinVar dbSNP
10g.119676903A>CCA378297129BAG3c.1349A>C (p.Lys450Thr)
c.1346A>C (p.Lys449Thr)
10g.119676903A>GCA378297130BAG3c.1349A>G (p.Lys450Arg)
c.1346A>G (p.Lys449Arg)
gnomAD v4
10g.119676903A>TCA378297128BAG3c.1349A>T (p.Lys450Met)
c.1346A>T (p.Lys449Met)
10g.119676904G>ACA471739532BAG3c.1350G>A (p.Lys450=)
c.1347G>A (p.Lys449=)
10g.119676904G>CCA378297131BAG3c.1350G>C (p.Lys450Asn)
c.1347G>C (p.Lys449Asn)
10g.119676904G>TCA378297132BAG3c.1350G>T (p.Lys450Asn)
c.1347G>T (p.Lys449Asn)
10g.119676905T>ACA378297133BAG3c.1351T>A (p.Tyr451Asn)
c.1348T>A (p.Tyr450Asn)
10g.119676905T>CCA378297134BAG3c.1351T>C (p.Tyr451His)
c.1348T>C (p.Tyr450His)
10g.119676905T>GCA378297135BAG3c.1351T>G (p.Tyr451Asp)
c.1348T>G (p.Tyr450Asp)
10g.119676906A>CCA378297136BAG3c.1352A>C (p.Tyr451Ser)
c.1349A>C (p.Tyr450Ser)
10g.119676906A>GCA378297137BAG3c.1352A>G (p.Tyr451Cys)
c.1349A>G (p.Tyr450Cys)
10g.119676906A>TCA378297138BAG3c.1352A>T (p.Tyr451Phe)
c.1349A>T (p.Tyr450Phe)
gnomAD v4
10g.119676907C>ACA378297139BAG3c.1353C>A (p.Tyr451Ter)
c.1350C>A (p.Tyr450Ter)
ClinVar dbSNP
10g.119676907C>GCA378297140BAG3c.1353C>G (p.Tyr451Ter)
c.1350C>G (p.Tyr450Ter)
10g.119676907C>TCA471739537BAG3c.1353C>T (p.Tyr451=)
c.1350C>T (p.Tyr450=)
gnomAD v4
10g.119676908C>ACA378297141BAG3c.1354C>A (p.Leu452Met)
c.1351C>A (p.Leu451Met)
10g.119676908C=CA1940196756BAG3c.1354C= (p.Leu452=)
c.1351C= (p.Leu451=)
10g.119676908C>GCA378297142BAG3c.1354C>G (p.Leu452Val)
c.1351C>G (p.Leu451Val)
10g.119676908C>TCA5716535BAG3c.1354C>T (p.Leu452=)
c.1351C>T (p.Leu451=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676909T>ACA378297145BAG3c.1355T>A (p.Leu452Gln)
c.1352T>A (p.Leu451Gln)
10g.119676909T>CCA378297143BAG3c.1355T>C (p.Leu452Pro)
c.1352T>C (p.Leu451Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676909T>GCA378297144BAG3c.1355T>G (p.Leu452Arg)
c.1352T>G (p.Leu451Arg)
10g.119676909T=CA1940196757BAG3c.1355T= (p.Leu452=)
c.1352T= (p.Leu451=)
10g.119676910G>ACA471739538BAG3c.1356G>A (p.Leu452=)
c.1353G>A (p.Leu451=)
ClinVar dbSNP gnomAD v4
10g.119676910G>CCA471739539BAG3c.1356G>C (p.Leu452=)
c.1353G>C (p.Leu451=)
10g.119676910G>TCA471739541BAG3c.1356G>T (p.Leu452=)
c.1353G>T (p.Leu451=)
10g.119676911A>CCA378297146BAG3c.1357A>C (p.Met453Leu)
c.1354A>C (p.Met452Leu)
10g.119676911A>GCA378297147BAG3c.1357A>G (p.Met453Val)
c.1354A>G (p.Met452Val)
10g.119676911A>TCA378297148BAG3c.1357A>T (p.Met453Leu)
c.1354A>T (p.Met452Leu)
10g.119676912T>ACA378297149BAG3c.1358T>A (p.Met453Lys)
c.1355T>A (p.Met452Lys)
10g.119676912T>CCA378297150BAG3c.1358T>C (p.Met453Thr)
c.1355T>C (p.Met452Thr)
10g.119676912T>GCA378297151BAG3c.1358T>G (p.Met453Arg)
c.1355T>G (p.Met452Arg)
10g.119676913G>ACA378297152BAG3c.1359G>A (p.Met453Ile)
c.1356G>A (p.Met452Ile)
gnomAD v4
10g.119676913G>CCA378297153BAG3c.1359G>C (p.Met453Ile)
c.1356G>C (p.Met452Ile)
10g.119676913G>TCA378297154BAG3c.1359G>T (p.Met453Ile)
c.1356G>T (p.Met452Ile)
10g.119676914A=CA1940196758BAG3c.1360A= (p.Ile454=)
c.1357A= (p.Ile453=)
10g.119676914A>CCA378297155BAG3c.1360A>C (p.Ile454Leu)
c.1357A>C (p.Ile453Leu)
10g.119676914A>GCA378297156BAG3c.1360A>G (p.Ile454Val)
c.1357A>G (p.Ile453Val)
dbSNP
10g.119676914A>TCA378297157BAG3c.1360A>T (p.Ile454Phe)
c.1357A>T (p.Ile453Phe)
10g.119676915T>ACA378297159BAG3c.1361T>A (p.Ile454Asn)
c.1358T>A (p.Ile453Asn)
dbSNP
10g.119676915T>CCA378297160BAG3c.1361T>C (p.Ile454Thr)
c.1358T>C (p.Ile453Thr)
ClinVar
10g.119676915T>GCA378297158BAG3c.1361T>G (p.Ile454Ser)
c.1358T>G (p.Ile453Ser)
10g.119676915T=CA1940196759BAG3c.1361T= (p.Ile454=)
c.1358T= (p.Ile453=)
10g.119676916C>ACA471739542BAG3c.1362C>A (p.Ile454=)
c.1359C>A (p.Ile453=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676916C=CA1940196760BAG3c.1362C= (p.Ile454=)
c.1359C= (p.Ile453=)
10g.119676916C>GCA378297161BAG3c.1362C>G (p.Ile454Met)
c.1359C>G (p.Ile453Met)
ClinVar dbSNP gnomAD v4
10g.119676916C>TCA5716536BAG3c.1362C>T (p.Ile454=)
c.1359C>T (p.Ile453=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676917G>ACA135016BAG3c.1363G>A (p.Glu455Lys)
c.1360G>A (p.Glu454Lys)
ClinVar dbSNP
10g.119676917G>CCA378297162BAG3c.1363G>C (p.Glu455Gln)
c.1360G>C (p.Glu454Gln)
10g.119676917G=CA1940196761BAG3c.1363G= (p.Glu455=)
c.1360G= (p.Glu454=)
10g.119676917G>TCA378297163BAG3c.1363G>T (p.Glu455Ter)
c.1360G>T (p.Glu454Ter)
10g.119676918A>CCA378297164BAG3c.1364A>C (p.Glu455Ala)
c.1361A>C (p.Glu454Ala)
10g.119676918A>GCA378297165BAG3c.1364A>G (p.Glu455Gly)
c.1361A>G (p.Glu454Gly)
10g.119676918A>TCA378297166BAG3c.1364A>T (p.Glu455Val)
c.1361A>T (p.Glu454Val)
10g.119676919A=CA1940196762BAG3c.1365A= (p.Glu455=)
c.1362A= (p.Glu454=)
10g.119676919A>CCA378297167BAG3c.1365A>C (p.Glu455Asp)
c.1362A>C (p.Glu454Asp)
10g.119676919A>GCA471739543BAG3c.1365A>G (p.Glu455=)
c.1362A>G (p.Glu454=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676919A>TCA378297168BAG3c.1365A>T (p.Glu455Asp)
c.1362A>T (p.Glu454Asp)
10g.119676920G>ACA378297169BAG3c.1366G>A (p.Glu456Lys)
c.1363G>A (p.Glu455Lys)
ClinVar
10g.119676920G>CCA378297170BAG3c.1366G>C (p.Glu456Gln)
c.1363G>C (p.Glu455Gln)
10g.119676920G>TCA378297171BAG3c.1366G>T (p.Glu456Ter)
c.1363G>T (p.Glu455Ter)
10g.119676921A>CCA378297172BAG3c.1367A>C (p.Glu456Ala)
c.1364A>C (p.Glu455Ala)
10g.119676921A>GCA378297173BAG3c.1367A>G (p.Glu456Gly)
c.1364A>G (p.Glu455Gly)
10g.119676921A>TCA378297174BAG3c.1367A>T (p.Glu456Val)
c.1364A>T (p.Glu455Val)
10g.119676922G>ACA471739544BAG3c.1368G>A (p.Glu456=)
c.1365G>A (p.Glu455=)
COSMIC
10g.119676922G>CCA378297176BAG3c.1368G>C (p.Glu456Asp)
c.1365G>C (p.Glu455Asp)
ClinVar
10g.119676922G>TCA378297175BAG3c.1368G>T (p.Glu456Asp)
c.1365G>T (p.Glu455Asp)
10g.119676923T>ACA378297177BAG3c.1369T>A (p.Tyr457Asn)
c.1366T>A (p.Tyr456Asn)
10g.119676923T>CCA378297178BAG3c.1369T>C (p.Tyr457His)
c.1366T>C (p.Tyr456His)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676923T>GCA378297179BAG3c.1369T>G (p.Tyr457Asp)
c.1366T>G (p.Tyr456Asp)
10g.119676923T=CA1940196763BAG3c.1369T= (p.Tyr457=)
c.1366T= (p.Tyr456=)
10g.119676924A>CCA378297180BAG3c.1370A>C (p.Tyr457Ser)
c.1367A>C (p.Tyr456Ser)
10g.119676924A>GCA378297181BAG3c.1370A>G (p.Tyr457Cys)
c.1367A>G (p.Tyr456Cys)
10g.119676924A>TCA378297182BAG3c.1370A>T (p.Tyr457Phe)
c.1367A>T (p.Tyr456Phe)
10g.119676925T>ACA378297183BAG3c.1371T>A (p.Tyr457Ter)
c.1368T>A (p.Tyr456Ter)
10g.119676925T>CCA471739548BAG3c.1371T>C (p.Tyr457=)
c.1368T>C (p.Tyr456=)
10g.119676925T>GCA378297184BAG3c.1371T>G (p.Tyr457Ter)
c.1368T>G (p.Tyr456Ter)
10g.119676926T>ACA378297185BAG3c.1372T>A (p.Leu458Met)
c.1369T>A (p.Leu457Met)
10g.119676926T>CCA471739549BAG3c.1372T>C (p.Leu458=)
c.1369T>C (p.Leu457=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119676926T>GCA378297186BAG3c.1372T>G (p.Leu458Val)
c.1369T>G (p.Leu457Val)
10g.119676926T=CA1940196764BAG3c.1372T= (p.Leu458=)
c.1369T= (p.Leu457=)

Number of alleles fetched