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.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=)
10g.119676927T>ACA378297187BAG3c.1373T>A (p.Leu458Ter)
c.1370T>A (p.Leu457Ter)
10g.119676927T>CCA378297188BAG3c.1373T>C (p.Leu458Ser)
c.1370T>C (p.Leu457Ser)
10g.119676927T>GCA378297189BAG3c.1373T>G (p.Leu458Trp)
c.1370T>G (p.Leu457Trp)
10g.119676928G>ACA471739552BAG3c.1374G>A (p.Leu458=)
c.1371G>A (p.Leu457=)
10g.119676928G>CCA378297190BAG3c.1374G>C (p.Leu458Phe)
c.1371G>C (p.Leu457Phe)
10g.119676928G>TCA378297191BAG3c.1374G>T (p.Leu458Phe)
c.1371G>T (p.Leu457Phe)
gnomAD v4
10g.119676929A>CCA378297192BAG3c.1375A>C (p.Thr459Pro)
c.1372A>C (p.Thr458Pro)
10g.119676929A>GCA378297193BAG3c.1375A>G (p.Thr459Ala)
c.1372A>G (p.Thr458Ala)
10g.119676929A>TCA378297194BAG3c.1375A>T (p.Thr459Ser)
c.1372A>T (p.Thr458Ser)
10g.119676930C>ACA378297195BAG3c.1376C>A (p.Thr459Asn)
c.1373C>A (p.Thr458Asn)
10g.119676930C>GCA378297196BAG3c.1376C>G (p.Thr459Ser)
c.1373C>G (p.Thr458Ser)
10g.119676930C>TCA378297197BAG3c.1376C>T (p.Thr459Ile)
c.1373C>T (p.Thr458Ile)
10g.119676931C>ACA471739557BAG3c.1377C>A (p.Thr459=)
c.1374C>A (p.Thr458=)
dbSNP
10g.119676931C=CA1940196765BAG3c.1377C= (p.Thr459=)
c.1374C= (p.Thr458=)
10g.119676931C>GCA471739555BAG3c.1377C>G (p.Thr459=)
c.1374C>G (p.Thr458=)
10g.119676931C>TCA471739554BAG3c.1377C>T (p.Thr459=)
c.1374C>T (p.Thr458=)
10g.119676932A>CCA378297198BAG3c.1378A>C (p.Lys460Gln)
c.1375A>C (p.Lys459Gln)
10g.119676932A>GCA378297199BAG3c.1378A>G (p.Lys460Glu)
c.1375A>G (p.Lys459Glu)
10g.119676932A>TCA378297200BAG3c.1378A>T (p.Lys460Ter)
c.1375A>T (p.Lys459Ter)
10g.119676933A=CA1940196766BAG3c.1379A= (p.Lys460=)
c.1376A= (p.Lys459=)
10g.119676933A>CCA378297201BAG3c.1379A>C (p.Lys460Thr)
c.1376A>C (p.Lys459Thr)
10g.119676933A>GCA378297202BAG3c.1379A>G (p.Lys460Arg)
c.1376A>G (p.Lys459Arg)
ClinVar dbSNP
10g.119676933A>TCA378297203BAG3c.1379A>T (p.Lys460Ile)
c.1376A>T (p.Lys459Ile)
10g.119676934A=CA1940196767BAG3c.1380A= (p.Lys460=)
c.1377A= (p.Lys459=)
10g.119676934A>CCA378297205BAG3c.1380A>C (p.Lys460Asn)
c.1377A>C (p.Lys459Asn)
10g.119676934A>GCA5716537BAG3c.1380A>G (p.Lys460=)
c.1377A>G (p.Lys459=)
dbSNP ExAC gnomAD v2
10g.119676934A>TCA378297204BAG3c.1380A>T (p.Lys460Asn)
c.1377A>T (p.Lys459Asn)
10g.119676935G>ACA378297206BAG3c.1381G>A (p.Glu461Lys)
c.1378G>A (p.Glu460Lys)
10g.119676935G>CCA378297207BAG3c.1381G>C (p.Glu461Gln)
c.1378G>C (p.Glu460Gln)
10g.119676935G>TCA378297208BAG3c.1381G>T (p.Glu461Ter)
c.1378G>T (p.Glu460Ter)
gnomAD v4
10g.119676936A>CCA378297209BAG3c.1382A>C (p.Glu461Ala)
c.1379A>C (p.Glu460Ala)
10g.119676936A>GCA378297210BAG3c.1382A>G (p.Glu461Gly)
c.1379A>G (p.Glu460Gly)
ClinVar
10g.119676936A>TCA378297211BAG3c.1382A>T (p.Glu461Val)
c.1379A>T (p.Glu460Val)
gnomAD v4 COSMIC
10g.119676937G>ACA471739563BAG3c.1383G>A (p.Glu461=)
c.1380G>A (p.Glu460=)
10g.119676937G>CCA378297212BAG3c.1383G>C (p.Glu461Asp)
c.1380G>C (p.Glu460Asp)
10g.119676937G>TCA378297213BAG3c.1383G>T (p.Glu461Asp)
c.1380G>T (p.Glu460Asp)
10g.119676938C>ACA378297214BAG3c.1384C>A (p.Leu462Met)
c.1381C>A (p.Leu461Met)
10g.119676938C>GCA378297215BAG3c.1384C>G (p.Leu462Val)
c.1381C>G (p.Leu461Val)
10g.119676938C>TCA471739567BAG3c.1384C>T (p.Leu462=)
c.1381C>T (p.Leu461=)
10g.119676939T>ACA378297216BAG3c.1385T>A (p.Leu462Gln)
c.1382T>A (p.Leu461Gln)
10g.119676939T>CCA261131BAG3c.1385T>C (p.Leu462Pro)
c.1382T>C (p.Leu461Pro)
ClinVar dbSNP
10g.119676939T>GCA378297217BAG3c.1385T>G (p.Leu462Arg)
c.1382T>G (p.Leu461Arg)
10g.119676939T=CA1940196768BAG3c.1385T= (p.Leu462=)
c.1382T= (p.Leu461=)
10g.119676940G>ACA471739569BAG3c.1386G>A (p.Leu462=)
c.1383G>A (p.Leu461=)
10g.119676940G>CCA471739570BAG3c.1386G>C (p.Leu462=)
c.1383G>C (p.Leu461=)
10g.119676940G>TCA471739571BAG3c.1386G>T (p.Leu462=)
c.1383G>T (p.Leu461=)
COSMIC
10g.119676941C>ACA378297219BAG3c.1387C>A (p.Leu463Met)
c.1384C>A (p.Leu462Met)
10g.119676941C>GCA378297218BAG3c.1387C>G (p.Leu463Val)
c.1384C>G (p.Leu462Val)
10g.119676941C>TCA471739573BAG3c.1387C>T (p.Leu463=)
c.1384C>T (p.Leu462=)
10g.119676942T>ACA378297220BAG3c.1388T>A (p.Leu463Gln)
c.1385T>A (p.Leu462Gln)
10g.119676942T>CCA378297221BAG3c.1388T>C (p.Leu463Pro)
c.1385T>C (p.Leu462Pro)
10g.119676942T>GCA378297222BAG3c.1388T>G (p.Leu463Arg)
c.1385T>G (p.Leu462Arg)
10g.119676943G>ACA214225196BAG3c.1389G>A (p.Leu463=)
c.1386G>A (p.Leu462=)
dbSNP
10g.119676943G>CCA471739574BAG3c.1389G>C (p.Leu463=)
c.1386G>C (p.Leu462=)
10g.119676943G=CA1940196769BAG3c.1389G= (p.Leu463=)
c.1386G= (p.Leu462=)
10g.119676943G>TCA471739575BAG3c.1389G>T (p.Leu463=)
c.1386G>T (p.Leu462=)
10g.119676944G>ACA378297223BAG3c.1390G>A (p.Ala464Thr)
c.1387G>A (p.Ala463Thr)
10g.119676944G>CCA378297224BAG3c.1390G>C (p.Ala464Pro)
c.1387G>C (p.Ala463Pro)
10g.119676944G>TCA378297225BAG3c.1390G>T (p.Ala464Ser)
c.1387G>T (p.Ala463Ser)
10g.119676945C>ACA378297226BAG3c.1391C>A (p.Ala464Asp)
c.1388C>A (p.Ala463Asp)
10g.119676945C>GCA378297227BAG3c.1391C>G (p.Ala464Gly)
c.1388C>G (p.Ala463Gly)
10g.119676945C>TCA378297228BAG3c.1391C>T (p.Ala464Val)
c.1388C>T (p.Ala463Val)
10g.119676946C>ACA471739580BAG3c.1392C>A (p.Ala464=)
c.1389C>A (p.Ala463=)
10g.119676946C>GCA471739581BAG3c.1392C>G (p.Ala464=)
c.1389C>G (p.Ala463=)
10g.119676946C>TCA471739582BAG3c.1392C>T (p.Ala464=)
c.1389C>T (p.Ala463=)
10g.119676947C>ACA378297229BAG3c.1393C>A (p.Leu465Met)
c.1390C>A (p.Leu464Met)
gnomAD v4
10g.119676947C>GCA378297230BAG3c.1393C>G (p.Leu465Val)
c.1390C>G (p.Leu464Val)
10g.119676947C>TCA471739584BAG3c.1393C>T (p.Leu465=)
c.1390C>T (p.Leu464=)
10g.119676948T>ACA378297231BAG3c.1394T>A (p.Leu465Gln)
c.1391T>A (p.Leu464Gln)
10g.119676948T>CCA378297232BAG3c.1394T>C (p.Leu465Pro)
c.1391T>C (p.Leu464Pro)
ClinVar dbSNP
10g.119676948T>GCA378297233BAG3c.1394T>G (p.Leu465Arg)
c.1391T>G (p.Leu464Arg)
10g.119676948T=CA1940196770BAG3c.1394T= (p.Leu465=)
c.1391T= (p.Leu464=)
10g.119676949G>ACA471739585BAG3c.1395G>A (p.Leu465=)
c.1392G>A (p.Leu464=)
gnomAD v4
10g.119676949G>CCA471739587BAG3c.1395G>C (p.Leu465=)
c.1392G>C (p.Leu464=)
10g.119676949G>TCA471739586BAG3c.1395G>T (p.Leu465=)
c.1392G>T (p.Leu464=)
10g.119676950G>ACA378297236BAG3c.1396G>A (p.Asp466Asn)
c.1393G>A (p.Asp465Asn)
ClinVar dbSNP
10g.119676950G>CCA378297235BAG3c.1396G>C (p.Asp466His)
c.1393G>C (p.Asp465His)
10g.119676950G=CA1940196771BAG3c.1396G= (p.Asp466=)
c.1393G= (p.Asp465=)
10g.119676950G>TCA378297234BAG3c.1396G>T (p.Asp466Tyr)
c.1393G>T (p.Asp465Tyr)
10g.119676951A>CCA378297237BAG3c.1397A>C (p.Asp466Ala)
c.1394A>C (p.Asp465Ala)
10g.119676951A>GCA378297238BAG3c.1397A>G (p.Asp466Gly)
c.1394A>G (p.Asp465Gly)
10g.119676951A>TCA378297239BAG3c.1397A>T (p.Asp466Val)
c.1394A>T (p.Asp465Val)
ClinVar
10g.119676952T>ACA378297240BAG3c.1398T>A (p.Asp466Glu)
c.1395T>A (p.Asp465Glu)
10g.119676952T>CCA471739393BAG3c.1398T>C (p.Asp466=)
c.1395T>C (p.Asp465=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676952T>GCA378297241BAG3c.1398T>G (p.Asp466Glu)
c.1395T>G (p.Asp465Glu)
10g.119676952T=CA1940196772BAG3c.1398T= (p.Asp466=)
c.1395T= (p.Asp465=)
10g.119676953T>ACA378297242BAG3c.1399T>A (p.Ser467Thr)
c.1396T>A (p.Ser466Thr)
10g.119676953T>CCA378297243BAG3c.1399T>C (p.Ser467Pro)
c.1396T>C (p.Ser466Pro)
10g.119676953T>GCA378297244BAG3c.1399T>G (p.Ser467Ala)
c.1396T>G (p.Ser466Ala)
10g.119676954C>ACA378297245BAG3c.1400C>A (p.Ser467Ter)
c.1397C>A (p.Ser466Ter)
10g.119676954C>GCA378297246BAG3c.1400C>G (p.Ser467Ter)
c.1397C>G (p.Ser466Ter)
10g.119676954C>TCA378297247BAG3c.1400C>T (p.Ser467Leu)
c.1397C>T (p.Ser466Leu)
gnomAD v4
10g.119676955A=CA1940196773BAG3c.1401A= (p.Ser467=)
c.1398A= (p.Ser466=)
10g.119676955A>CCA471739395BAG3c.1401A>C (p.Ser467=)
c.1398A>C (p.Ser466=)
dbSNP gnomAD v3 gnomAD v4
10g.119676955A>GCA471739396BAG3c.1401A>G (p.Ser467=)
c.1398A>G (p.Ser466=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676955A>TCA471739397BAG3c.1401A>T (p.Ser467=)
c.1398A>T (p.Ser466=)
10g.119676956G>ACA378297248BAG3c.1402G>A (p.Val468Met)
c.1399G>A (p.Val467Met)
ClinVar
10g.119676956G>CCA378297249BAG3c.1402G>C (p.Val468Leu)
c.1399G>C (p.Val467Leu)
10g.119676956G>TCA378297250BAG3c.1402G>T (p.Val468Leu)
c.1399G>T (p.Val467Leu)
10g.119676957T>ACA378297252BAG3c.1403T>A (p.Val468Glu)
c.1400T>A (p.Val467Glu)
10g.119676957T>CCA378297253BAG3c.1403T>C (p.Val468Ala)
c.1400T>C (p.Val467Ala)
gnomAD v4
10g.119676957T>GCA378297251BAG3c.1403T>G (p.Val468Gly)
c.1400T>G (p.Val467Gly)
10g.119676958G>ACA471739398BAG3c.1404G>A (p.Val468=)
c.1401G>A (p.Val467=)
dbSNP gnomAD v4
10g.119676958G>CCA471739400BAG3c.1404G>C (p.Val468=)
c.1401G>C (p.Val467=)
10g.119676958G=CA1940196774BAG3c.1404G= (p.Val468=)
c.1401G= (p.Val467=)
10g.119676958G>TCA471739401BAG3c.1404G>T (p.Val468=)
c.1401G>T (p.Val467=)
10g.119676959G>ACA378297254BAG3c.1405G>A (p.Asp469Asn)
c.1402G>A (p.Asp468Asn)
10g.119676959G>CCA378297255BAG3c.1405G>C (p.Asp469His)
c.1402G>C (p.Asp468His)
10g.119676959G>TCA378297256BAG3c.1405G>T (p.Asp469Tyr)
c.1402G>T (p.Asp468Tyr)
10g.119676960A=CA1940196775BAG3c.1406A= (p.Asp469=)
c.1403A= (p.Asp468=)
10g.119676960A>CCA5716538BAG3c.1406A>C (p.Asp469Ala)
c.1403A>C (p.Asp468Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676960A>GCA378297257BAG3c.1406A>G (p.Asp469Gly)
c.1403A>G (p.Asp468Gly)
10g.119676960A>TCA378297258BAG3c.1406A>T (p.Asp469Val)
c.1403A>T (p.Asp468Val)
10g.119676961C>ACA378297259BAG3c.1407C>A (p.Asp469Glu)
c.1404C>A (p.Asp468Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676961C=CA1940196776BAG3c.1407C= (p.Asp469=)
c.1404C= (p.Asp468=)
10g.119676961C>GCA378297260BAG3c.1407C>G (p.Asp469Glu)
c.1404C>G (p.Asp468Glu)
dbSNP gnomAD v4
10g.119676961C>TCA471739404BAG3c.1407C>T (p.Asp469=)
c.1404C>T (p.Asp468=)
gnomAD v4
10g.119676964delCA2499220177BAG3c.1410del (p.Glu471ArgfsTer?)
c.1407del (p.Glu470ArgfsTer?)
ClinVar dbSNP
10g.119676962C>ACA5716539BAG3c.1408C>A (p.Pro470Thr)
c.1405C>A (p.Pro469Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676962C=CA1940196777BAG3c.1408C= (p.Pro470=)
c.1405C= (p.Pro469=)
10g.119676962C>GCA378297261BAG3c.1408C>G (p.Pro470Ala)
c.1405C>G (p.Pro469Ala)
10g.119676962C>TCA378297262BAG3c.1408C>T (p.Pro470Ser)
c.1405C>T (p.Pro469Ser)
ClinVar dbSNP
10g.119676963C>ACA5716540BAG3c.1409C>A (p.Pro470His)
c.1406C>A (p.Pro469His)
dbSNP ExAC
10g.119676963C=CA1940196778BAG3c.1409C= (p.Pro470=)
c.1406C= (p.Pro469=)
10g.119676963C>GCA378297263BAG3c.1409C>G (p.Pro470Arg)
c.1406C>G (p.Pro469Arg)
10g.119676963C>TCA378297264BAG3c.1409C>T (p.Pro470Leu)
c.1406C>T (p.Pro469Leu)
ClinVar dbSNP
10g.119676964C>ACA471739406BAG3c.1410C>A (p.Pro470=)
c.1407C>A (p.Pro469=)
10g.119676964C=CA1940196779BAG3c.1410C= (p.Pro470=)
c.1407C= (p.Pro469=)
10g.119676964C>GCA5716541BAG3c.1410C>G (p.Pro470=)
c.1407C>G (p.Pro469=)
dbSNP ExAC gnomAD v4
10g.119676964C>TCA5716542BAG3c.1410C>T (p.Pro470=)
c.1407C>T (p.Pro469=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676965G>ACA5716543BAG3c.1411G>A (p.Glu471Lys)
c.1408G>A (p.Glu470Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676965G>CCA378297265BAG3c.1411G>C (p.Glu471Gln)
c.1408G>C (p.Glu470Gln)
ClinVar dbSNP
10g.119676965G=CA1940196780BAG3c.1411G= (p.Glu471=)
c.1408G= (p.Glu470=)
10g.119676965G>TCA378297266BAG3c.1411G>T (p.Glu471Ter)
c.1408G>T (p.Glu470Ter)
10g.119676966A=CA1940196781BAG3c.1412A= (p.Glu471=)
c.1409A= (p.Glu470=)
10g.119676966A>CCA378297267BAG3c.1412A>C (p.Glu471Ala)
c.1409A>C (p.Glu470Ala)
10g.119676966A>GCA5716544BAG3c.1412A>G (p.Glu471Gly)
c.1409A>G (p.Glu470Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676966A>TCA378297268BAG3c.1412A>T (p.Glu471Val)
c.1409A>T (p.Glu470Val)
10g.119676967G>ACA471739409BAG3c.1413G>A (p.Glu471=)
c.1410G>A (p.Glu470=)
ClinVar dbSNP gnomAD v4
10g.119676967G>CCA378297269BAG3c.1413G>C (p.Glu471Asp)
c.1410G>C (p.Glu470Asp)
gnomAD v4
10g.119676967G=CA1940196782BAG3c.1413G= (p.Glu471=)
c.1410G= (p.Glu470=)
10g.119676967G>TCA378297270BAG3c.1413G>T (p.Glu471Asp)
c.1410G>T (p.Glu470Asp)
gnomAD v4 COSMIC
10g.119676968G>ACA378297271BAG3c.1414G>A (p.Gly472Arg)
c.1411G>A (p.Gly471Arg)
ClinVar dbSNP gnomAD v4
10g.119676968G>CCA378297272BAG3c.1414G>C (p.Gly472Arg)
c.1411G>C (p.Gly471Arg)
10g.119676968G=CA1940196783BAG3c.1414G= (p.Gly472=)
c.1411G= (p.Gly471=)
10g.119676968G>TCA378297273BAG3c.1414G>T (p.Gly472Ter)
c.1411G>T (p.Gly471Ter)
ClinVar
10g.119676969G>ACA378297276BAG3c.1415G>A (p.Gly472Glu)
c.1412G>A (p.Gly471Glu)
dbSNP
10g.119676969G>CCA378297275BAG3c.1415G>C (p.Gly472Ala)
c.1412G>C (p.Gly471Ala)
gnomAD v4
10g.119676969G=CA1940196784BAG3c.1415G= (p.Gly472=)
c.1412G= (p.Gly471=)
10g.119676969G>TCA378297274BAG3c.1415G>T (p.Gly472Val)
c.1412G>T (p.Gly471Val)
10g.119676970A=CA1940196785BAG3c.1416A= (p.Gly472=)
c.1413A= (p.Gly471=)
10g.119676970A>CCA471739414BAG3c.1416A>C (p.Gly472=)
c.1413A>C (p.Gly471=)
10g.119676970A>GCA5716545BAG3c.1416A>G (p.Gly472=)
c.1413A>G (p.Gly471=)
dbSNP ExAC gnomAD v4
10g.119676970A>TCA471739413BAG3c.1416A>T (p.Gly472=)
c.1413A>T (p.Gly471=)
10g.119676970_119676971delCA645568607BAG3c.1416_1417del (p.Arg473SerfsTer22)
c.1413_1414del (p.Arg472SerfsTer22)
COSMIC
10g.119676971C>ACA471739416BAG3c.1417C>A (p.Arg473=)
c.1414C>A (p.Arg472=)
10g.119676971C=CA1940196786BAG3c.1417C= (p.Arg473=)
c.1414C= (p.Arg472=)
10g.119676971C>GCA5716546BAG3c.1417C>G (p.Arg473Gly)
c.1414C>G (p.Arg472Gly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676971C>TCA378297277BAG3c.1417C>T (p.Arg473Ter)
c.1414C>T (p.Arg472Ter)
ClinVar dbSNP COSMIC
10g.119676972G>ACA5716547BAG3c.1418G>A (p.Arg473Gln)
c.1415G>A (p.Arg472Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676972G>CCA378297278BAG3c.1418G>C (p.Arg473Pro)
c.1415G>C (p.Arg472Pro)
10g.119676972G=CA1940196787BAG3c.1418G= (p.Arg473=)
c.1415G= (p.Arg472=)
10g.119676972G>TCA378297279BAG3c.1418G>T (p.Arg473Leu)
c.1415G>T (p.Arg472Leu)
gnomAD v4
10g.119676972dupCA915948735BAG3c.1418dup (p.Ala474SerfsTer22)
c.1415dup (p.Ala473SerfsTer22)
ClinVar dbSNP
10g.119676973A>CCA471739419BAG3c.1419A>C (p.Arg473=)
c.1416A>C (p.Arg472=)
10g.119676973A>GCA471739418BAG3c.1419A>G (p.Arg473=)
c.1416A>G (p.Arg472=)
COSMIC
10g.119676973A>TCA471739417BAG3c.1419A>T (p.Arg473=)
c.1416A>T (p.Arg472=)
10g.119676974G>ACA378297280BAG3c.1420G>A (p.Ala474Thr)
c.1417G>A (p.Ala473Thr)
ClinVar dbSNP gnomAD v4
10g.119676974G>CCA378297281BAG3c.1420G>C (p.Ala474Pro)
c.1417G>C (p.Ala473Pro)
10g.119676974G>TCA378297282BAG3c.1420G>T (p.Ala474Ser)
c.1417G>T (p.Ala473Ser)
10g.119676975C>ACA378297283BAG3c.1421C>A (p.Ala474Asp)
c.1418C>A (p.Ala473Asp)
10g.119676975C=CA1940196788BAG3c.1421C= (p.Ala474=)
c.1418C= (p.Ala473=)
10g.119676975C>GCA378297284BAG3c.1421C>G (p.Ala474Gly)
c.1418C>G (p.Ala473Gly)
10g.119676975C>TCA378297285BAG3c.1421C>T (p.Ala474Val)
c.1418C>T (p.Ala473Val)
dbSNP
10g.119676976C>ACA471739421BAG3c.1422C>A (p.Ala474=)
c.1419C>A (p.Ala473=)
10g.119676976C=CA1940196789BAG3c.1422C= (p.Ala474=)
c.1419C= (p.Ala473=)
10g.119676976C>GCA471739422BAG3c.1422C>G (p.Ala474=)
c.1419C>G (p.Ala473=)
dbSNP gnomAD v4
10g.119676976C>TCA184800BAG3c.1422C>T (p.Ala474=)
c.1419C>T (p.Ala473=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676977G>ACA5716548BAG3c.1423G>A (p.Asp475Asn)
c.1420G>A (p.Asp474Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676977G>CCA378297286BAG3c.1423G>C (p.Asp475His)
c.1420G>C (p.Asp474His)
10g.119676977G=CA1940196790BAG3c.1423G= (p.Asp475=)
c.1420G= (p.Asp474=)
10g.119676977G>TCA378297287BAG3c.1423G>T (p.Asp475Tyr)
c.1420G>T (p.Asp474Tyr)
10g.119676978A=CA1940196791BAG3c.1424A= (p.Asp475=)
c.1421A= (p.Asp474=)
10g.119676978A>CCA378297289BAG3c.1424A>C (p.Asp475Ala)
c.1421A>C (p.Asp474Ala)
10g.119676978A>GCA5716549BAG3c.1424A>G (p.Asp475Gly)
c.1421A>G (p.Asp474Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676978A>TCA378297288BAG3c.1424A>T (p.Asp475Val)
c.1421A>T (p.Asp474Val)
10g.119676979T>ACA378297290BAG3c.1425T>A (p.Asp475Glu)
c.1422T>A (p.Asp474Glu)
ClinVar gnomAD v4
10g.119676979T>CCA5716550BAG3c.1425T>C (p.Asp475=)
c.1422T>C (p.Asp474=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676979T>GCA378297291BAG3c.1425T>G (p.Asp475Glu)
c.1422T>G (p.Asp474Glu)
10g.119676979T=CA1940196792BAG3c.1425T= (p.Asp475=)
c.1422T= (p.Asp474=)
10g.119676980G>ACA378297292BAG3c.1426G>A (p.Val476Met)
c.1423G>A (p.Val475Met)
dbSNP gnomAD v2
10g.119676980G>CCA378297293BAG3c.1426G>C (p.Val476Leu)
c.1423G>C (p.Val475Leu)
10g.119676980G=CA1940196793BAG3c.1426G= (p.Val476=)
c.1423G= (p.Val475=)
10g.119676980G>TCA378297294BAG3c.1426G>T (p.Val476Leu)
c.1423G>T (p.Val475Leu)
10g.119676981T>ACA378297295BAG3c.1427T>A (p.Val476Glu)
c.1424T>A (p.Val475Glu)
10g.119676981T>CCA378297296BAG3c.1427T>C (p.Val476Ala)
c.1424T>C (p.Val475Ala)
10g.119676981T>GCA378297297BAG3c.1427T>G (p.Val476Gly)
c.1424T>G (p.Val475Gly)
10g.119676982G>ACA471739428BAG3c.1428G>A (p.Val476=)
c.1425G>A (p.Val475=)
ClinVar dbSNP
10g.119676982G>CCA471739429BAG3c.1428G>C (p.Val476=)
c.1425G>C (p.Val475=)
10g.119676982G=CA1940196794BAG3c.1428G= (p.Val476=)
c.1425G= (p.Val475=)
10g.119676982G>TCA471739430BAG3c.1428G>T (p.Val476=)
c.1425G>T (p.Val475=)
10g.119676983C>ACA378297298BAG3c.1429C>A (p.Arg477Ser)
c.1426C>A (p.Arg476Ser)
COSMIC
10g.119676983C=CA1940196795BAG3c.1429C= (p.Arg477=)
c.1426C= (p.Arg476=)
10g.119676983C>GCA378297299BAG3c.1429C>G (p.Arg477Gly)
c.1426C>G (p.Arg476Gly)
gnomAD v4
10g.119676983C>TCA5716551BAG3c.1429C>T (p.Arg477Cys)
c.1426C>T (p.Arg476Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
10g.119676984G>ACA259793BAG3c.1430G>A (p.Arg477His)
c.1427G>A (p.Arg476His)
ClinVar dbSNP gnomAD v4 COSMIC
10g.119676984G>CCA378297300BAG3c.1430G>C (p.Arg477Pro)
c.1427G>C (p.Arg476Pro)
10g.119676984G=CA1940196796BAG3c.1430G= (p.Arg477=)
c.1427G= (p.Arg476=)
10g.119676984G>TCA378297301BAG3c.1430G>T (p.Arg477Leu)
c.1427G>T (p.Arg476Leu)
10g.119676985T>ACA471739433BAG3c.1431T>A (p.Arg477=)
c.1428T>A (p.Arg476=)
10g.119676985T>CCA471739435BAG3c.1431T>C (p.Arg477=)
c.1428T>C (p.Arg476=)
10g.119676985T>GCA471739436BAG3c.1431T>G (p.Arg477=)
c.1428T>G (p.Arg476=)
10g.119676986C>ACA378297303BAG3c.1432C>A (p.Gln478Lys)
c.1429C>A (p.Gln477Lys)
10g.119676986C>GCA378297304BAG3c.1432C>G (p.Gln478Glu)
c.1429C>G (p.Gln477Glu)
10g.119676986C>TCA378297302BAG3c.1432C>T (p.Gln478Ter)
c.1429C>T (p.Gln477Ter)
10g.119676987A>CCA378297305BAG3c.1433A>C (p.Gln478Pro)
c.1430A>C (p.Gln477Pro)
10g.119676987A>GCA378297306BAG3c.1433A>G (p.Gln478Arg)
c.1430A>G (p.Gln477Arg)
10g.119676987A>TCA378297307BAG3c.1433A>T (p.Gln478Leu)
c.1430A>T (p.Gln477Leu)
10g.119676988G>ACA471739440BAG3c.1434G>A (p.Gln478=)
c.1431G>A (p.Gln477=)
gnomAD v4
10g.119676988G>CCA378297308BAG3c.1434G>C (p.Gln478His)
c.1431G>C (p.Gln477His)
10g.119676988G>TCA378297309BAG3c.1434G>T (p.Gln478His)
c.1431G>T (p.Gln477His)
10g.119676989G>ACA378297310BAG3c.1435G>A (p.Ala479Thr)
c.1432G>A (p.Ala478Thr)
gnomAD v4
10g.119676989G>CCA378297311BAG3c.1435G>C (p.Ala479Pro)
c.1432G>C (p.Ala478Pro)
10g.119676989G>TCA378297312BAG3c.1435G>T (p.Ala479Ser)
c.1432G>T (p.Ala478Ser)
10g.119676990C>ACA378297313BAG3c.1436C>A (p.Ala479Asp)
c.1433C>A (p.Ala478Asp)
dbSNP gnomAD v4
10g.119676990C=CA1940196797BAG3c.1436C= (p.Ala479=)
c.1433C= (p.Ala478=)
10g.119676990C>GCA378297314BAG3c.1436C>G (p.Ala479Gly)
c.1433C>G (p.Ala478Gly)
10g.119676990C>TCA302591BAG3c.1436C>T (p.Ala479Val)
c.1433C>T (p.Ala478Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676991C>ACA471739443BAG3c.1437C>A (p.Ala479=)
c.1434C>A (p.Ala478=)
10g.119676991C>GCA471739444BAG3c.1437C>G (p.Ala479=)
c.1434C>G (p.Ala478=)
10g.119676991C>TCA471739442BAG3c.1437C>T (p.Ala479=)
c.1434C>T (p.Ala478=)
10g.119676992A=CA1940196798BAG3c.1438A= (p.Arg480=)
c.1435A= (p.Arg479=)
10g.119676992A>CCA471739445BAG3c.1438A>C (p.Arg480=)
c.1435A>C (p.Arg479=)
dbSNP
10g.119676992A>GCA378297315BAG3c.1438A>G (p.Arg480Gly)
c.1435A>G (p.Arg479Gly)
10g.119676992A>TCA378297316BAG3c.1438A>T (p.Arg480Trp)
c.1435A>T (p.Arg479Trp)
10g.119676993G>ACA378297319BAG3c.1439G>A (p.Arg480Lys)
c.1436G>A (p.Arg479Lys)
10g.119676993G>CCA378297317BAG3c.1439G>C (p.Arg480Thr)
c.1436G>C (p.Arg479Thr)
10g.119676993G>TCA378297318BAG3c.1439G>T (p.Arg480Met)
c.1436G>T (p.Arg479Met)
10g.119676994_119677004delCA2825001684BAG3c.1440_1450del (p.Arg480SerfsTer12)
c.1437_1447del (p.Arg479SerfsTer12)
ClinVar
10g.119676994G>ACA471739449BAG3c.1440G>A (p.Arg480=)
c.1437G>A (p.Arg479=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119676994G>CCA378297320BAG3c.1440G>C (p.Arg480Ser)
c.1437G>C (p.Arg479Ser)
10g.119676994G=CA1940196799BAG3c.1440G= (p.Arg480=)
c.1437G= (p.Arg479=)
10g.119676994G>TCA378297321BAG3c.1440G>T (p.Arg480Ser)
c.1437G>T (p.Arg479Ser)
10g.119676998_119676999delCA2695212842BAG3c.1444_1445del (p.Asp482ArgfsTer13)
c.1441_1442del (p.Asp481ArgfsTer13)
10g.119676995A>CCA471739450BAG3c.1441A>C (p.Arg481=)
c.1438A>C (p.Arg480=)
10g.119676995A>GCA378297322BAG3c.1441A>G (p.Arg481Gly)
c.1438A>G (p.Arg480Gly)
gnomAD v4
10g.119676995A>TCA378297323BAG3c.1441A>T (p.Arg481Ter)
c.1438A>T (p.Arg480Ter)
10g.119676996G>ACA378297324BAG3c.1442G>A (p.Arg481Lys)
c.1439G>A (p.Arg480Lys)
dbSNP
10g.119676996G>CCA378297325BAG3c.1442G>C (p.Arg481Thr)
c.1439G>C (p.Arg480Thr)
ClinVar
10g.119676996G=CA1940196800BAG3c.1442G= (p.Arg481=)
c.1439G= (p.Arg480=)
10g.119676996G>TCA378297326BAG3c.1442G>T (p.Arg481Ile)
c.1439G>T (p.Arg480Ile)
10g.119676997A>CCA378297327BAG3c.1443A>C (p.Arg481Ser)
c.1440A>C (p.Arg480Ser)
10g.119676997A>GCA471739452BAG3c.1443A>G (p.Arg481=)
c.1440A>G (p.Arg480=)
10g.119676997A>TCA378297328BAG3c.1443A>T (p.Arg481Ser)
c.1440A>T (p.Arg480Ser)
10g.119676998G>ACA378297329BAG3c.1444G>A (p.Asp482Asn)
c.1441G>A (p.Asp481Asn)
10g.119676998G>CCA378297330BAG3c.1444G>C (p.Asp482His)
c.1441G>C (p.Asp481His)
COSMIC
10g.119676998G>TCA378297331BAG3c.1444G>T (p.Asp482Tyr)
c.1441G>T (p.Asp481Tyr)
10g.119676999A>CCA378297332BAG3c.1445A>C (p.Asp482Ala)
c.1442A>C (p.Asp481Ala)
10g.119676999A>GCA378297334BAG3c.1445A>G (p.Asp482Gly)
c.1442A>G (p.Asp481Gly)
10g.119676999A>TCA378297333BAG3c.1445A>T (p.Asp482Val)
c.1442A>T (p.Asp481Val)
10g.119676999dupCA2740093566BAG3c.1445dup (p.Asp482GlufsTer14)
c.1442dup (p.Asp481GlufsTer14)
ClinVar
10g.119677000C>ACA378297335BAG3c.1446C>A (p.Asp482Glu)
c.1443C>A (p.Asp481Glu)
10g.119677000C=CA1940196801BAG3c.1446C= (p.Asp482=)
c.1443C= (p.Asp481=)
10g.119677000C>GCA5716553BAG3c.1446C>G (p.Asp482Glu)
c.1443C>G (p.Asp481Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677000C>TCA5716552BAG3c.1446C>T (p.Asp482=)
c.1443C>T (p.Asp481=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677001G>ACA5716554BAG3c.1447G>A (p.Gly483Ser)
c.1444G>A (p.Gly482Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677001G>CCA378297336BAG3c.1447G>C (p.Gly483Arg)
c.1444G>C (p.Gly482Arg)
10g.119677001G=CA1940196802BAG3c.1447G= (p.Gly483=)
c.1444G= (p.Gly482=)
10g.119677001G>TCA378297337BAG3c.1447G>T (p.Gly483Cys)
c.1444G>T (p.Gly482Cys)
10g.119677002G>ACA378297338BAG3c.1448G>A (p.Gly483Asp)
c.1445G>A (p.Gly482Asp)
10g.119677002G>CCA378297339BAG3c.1448G>C (p.Gly483Ala)
c.1445G>C (p.Gly482Ala)
10g.119677002G>TCA378297340BAG3c.1448G>T (p.Gly483Val)
c.1445G>T (p.Gly482Val)
10g.119677003T>ACA471739456BAG3c.1449T>A (p.Gly483=)
c.1446T>A (p.Gly482=)
10g.119677003T>CCA471739458BAG3c.1449T>C (p.Gly483=)
c.1446T>C (p.Gly482=)
dbSNP
10g.119677003T>GCA471739459BAG3c.1449T>G (p.Gly483=)
c.1446T>G (p.Gly482=)
ClinVar dbSNP
10g.119677003T=CA1940196803BAG3c.1449T= (p.Gly483=)
c.1446T= (p.Gly482=)
10g.119677004G>ACA378297341BAG3c.1450G>A (p.Val484Ile)
c.1447G>A (p.Val483Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119677004G>CCA378297342BAG3c.1450G>C (p.Val484Leu)
c.1447G>C (p.Val483Leu)
10g.119677004G=CA1940196804BAG3c.1450G= (p.Val484=)
c.1447G= (p.Val483=)
10g.119677004G>TCA378297343BAG3c.1450G>T (p.Val484Phe)
c.1447G>T (p.Val483Phe)
10g.119677005T>ACA378297344BAG3c.1451T>A (p.Val484Asp)
c.1448T>A (p.Val483Asp)
ClinVar dbSNP
10g.119677005T>CCA378297345BAG3c.1451T>C (p.Val484Ala)
c.1448T>C (p.Val483Ala)
10g.119677005T>GCA378297346BAG3c.1451T>G (p.Val484Gly)
c.1448T>G (p.Val483Gly)
10g.119677006C>ACA471739462BAG3c.1452C>A (p.Val484=)
c.1449C>A (p.Val483=)
ClinVar dbSNP
10g.119677006C=CA1940196805BAG3c.1452C= (p.Val484=)
c.1449C= (p.Val483=)
10g.119677006C>GCA471739464BAG3c.1452C>G (p.Val484=)
c.1449C>G (p.Val483=)
gnomAD v4
10g.119677006C>TCA471739465BAG3c.1452C>T (p.Val484=)
c.1449C>T (p.Val483=)
dbSNP gnomAD v4
10g.119677007A>CCA471739466BAG3c.1453A>C (p.Arg485=)
c.1450A>C (p.Arg484=)
10g.119677007A>GCA378297347BAG3c.1453A>G (p.Arg485Gly)
c.1450A>G (p.Arg484Gly)
ClinVar dbSNP
10g.119677007A>TCA378297348BAG3c.1453A>T (p.Arg485Trp)
c.1450A>T (p.Arg484Trp)
10g.119677008G>ACA378297349BAG3c.1454G>A (p.Arg485Lys)
c.1451G>A (p.Arg484Lys)
10g.119677008G>CCA378297350BAG3c.1454G>C (p.Arg485Thr)
c.1451G>C (p.Arg484Thr)
10g.119677008G>TCA378297351BAG3c.1454G>T (p.Arg485Met)
c.1451G>T (p.Arg484Met)
10g.119677009G>ACA214225269BAG3c.1455G>A (p.Arg485=)
c.1452G>A (p.Arg484=)
ClinVar dbSNP gnomAD v4
10g.119677009G>CCA378297352BAG3c.1455G>C (p.Arg485Ser)
c.1452G>C (p.Arg484Ser)
10g.119677009G=CA1940196806BAG3c.1455G= (p.Arg485=)
c.1452G= (p.Arg484=)
10g.119677009G>TCA378297353BAG3c.1455G>T (p.Arg485Ser)
c.1452G>T (p.Arg484Ser)
10g.119677010A>CCA378297354BAG3c.1456A>C (p.Lys486Gln)
c.1453A>C (p.Lys485Gln)
10g.119677010A>GCA378297355BAG3c.1456A>G (p.Lys486Glu)
c.1453A>G (p.Lys485Glu)
10g.119677010A>TCA378297356BAG3c.1456A>T (p.Lys486Ter)
c.1453A>T (p.Lys485Ter)
10g.119677011A=CA1940196807BAG3c.1457A= (p.Lys486=)
c.1454A= (p.Lys485=)
10g.119677011A>CCA378297357BAG3c.1457A>C (p.Lys486Thr)
c.1454A>C (p.Lys485Thr)
10g.119677011A>GCA5716555BAG3c.1457A>G (p.Lys486Arg)
c.1454A>G (p.Lys485Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677011A>TCA378297358BAG3c.1457A>T (p.Lys486Met)
c.1454A>T (p.Lys485Met)
10g.119677012G>ACA471739468BAG3c.1458G>A (p.Lys486=)
c.1455G>A (p.Lys485=)
dbSNP gnomAD v3 gnomAD v4
10g.119677012G>CCA378297359BAG3c.1458G>C (p.Lys486Asn)
c.1455G>C (p.Lys485Asn)
gnomAD v4
10g.119677012G=CA1940196808BAG3c.1458G= (p.Lys486=)
c.1455G= (p.Lys485=)
10g.119677012G>TCA378297360BAG3c.1458G>T (p.Lys486Asn)
c.1455G>T (p.Lys485Asn)
dbSNP
10g.119677013G>ACA378297361BAG3c.1459G>A (p.Val487Ile)
c.1456G>A (p.Val486Ile)
10g.119677013G>CCA378297363BAG3c.1459G>C (p.Val487Leu)
c.1456G>C (p.Val486Leu)
10g.119677013G>TCA378297362BAG3c.1459G>T (p.Val487Phe)
c.1456G>T (p.Val486Phe)
10g.119677014T>ACA378297364BAG3c.1460T>A (p.Val487Asp)
c.1457T>A (p.Val486Asp)
10g.119677014T>CCA378297365BAG3c.1460T>C (p.Val487Ala)
c.1457T>C (p.Val486Ala)
10g.119677014T>GCA378297366BAG3c.1460T>G (p.Val487Gly)
c.1457T>G (p.Val486Gly)
10g.119677015T>ACA471739470BAG3c.1461T>A (p.Val487=)
c.1458T>A (p.Val486=)
gnomAD v4
10g.119677015T>CCA471739471BAG3c.1461T>C (p.Val487=)
c.1458T>C (p.Val486=)
10g.119677015T>GCA471739472BAG3c.1461T>G (p.Val487=)
c.1458T>G (p.Val486=)
10g.119677016C>ACA378297367BAG3c.1462C>A (p.Gln488Lys)
c.1459C>A (p.Gln487Lys)
10g.119677016C>GCA378297368BAG3c.1462C>G (p.Gln488Glu)
c.1459C>G (p.Gln487Glu)
10g.119677016C>TCA378297369BAG3c.1462C>T (p.Gln488Ter)
c.1459C>T (p.Gln487Ter)
10g.119677017A>CCA378297370BAG3c.1463A>C (p.Gln488Pro)
c.1460A>C (p.Gln487Pro)
10g.119677017A>GCA378297371BAG3c.1463A>G (p.Gln488Arg)
c.1460A>G (p.Gln487Arg)
10g.119677017A>TCA378297372BAG3c.1463A>T (p.Gln488Leu)
c.1460A>T (p.Gln487Leu)
10g.119677018G>ACA471739475BAG3c.1464G>A (p.Gln488=)
c.1461G>A (p.Gln487=)
10g.119677018G>CCA378297373BAG3c.1464G>C (p.Gln488His)
c.1461G>C (p.Gln487His)
gnomAD v4
10g.119677018G>TCA378297374BAG3c.1464G>T (p.Gln488His)
c.1461G>T (p.Gln487His)
10g.119677019A>CCA378297377BAG3c.1465A>C (p.Thr489Pro)
c.1462A>C (p.Thr488Pro)
10g.119677019A>GCA378297376BAG3c.1465A>G (p.Thr489Ala)
c.1462A>G (p.Thr488Ala)
10g.119677019A>TCA378297375BAG3c.1465A>T (p.Thr489Ser)
c.1462A>T (p.Thr488Ser)
10g.119677020C>ACA378297378BAG3c.1466C>A (p.Thr489Asn)
c.1463C>A (p.Thr488Asn)
10g.119677020C>GCA378297379BAG3c.1466C>G (p.Thr489Ser)
c.1463C>G (p.Thr488Ser)
10g.119677020C>TCA378297380BAG3c.1466C>T (p.Thr489Ile)
c.1463C>T (p.Thr488Ile)

Number of alleles fetched