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.119676817A>CCA471739425BAG3c.1263A>C (p.Gly421=)
c.1260A>C (p.Gly420=)
ClinVar dbSNP
10g.119676817A>GCA471739426BAG3c.1263A>G (p.Gly421=)
c.1260A>G (p.Gly420=)
10g.119676817A>TCA471739427BAG3c.1263A>T (p.Gly421=)
c.1260A>T (p.Gly420=)
10g.119676818G>ACA5716523BAG3c.1264G>A (p.Val422Met)
c.1261G>A (p.Val421Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676818G>CCA5716524BAG3c.1264G>C (p.Val422Leu)
c.1261G>C (p.Val421Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119676818G=CA1940196714BAG3c.1264G= (p.Val422=)
c.1261G= (p.Val421=)
10g.119676818G>TCA378296944BAG3c.1264G>T (p.Val422Leu)
c.1261G>T (p.Val421Leu)
10g.119676819T>ACA378296945BAG3c.1265T>A (p.Val422Glu)
c.1262T>A (p.Val421Glu)
10g.119676819T>CCA378296946BAG3c.1265T>C (p.Val422Ala)
c.1262T>C (p.Val421Ala)
10g.119676819T>GCA378296947BAG3c.1265T>G (p.Val422Gly)
c.1262T>G (p.Val421Gly)
gnomAD v3 gnomAD v4
10g.119676819_119676829delinsTGCTGAAAGTGCA1940196715BAG3c.1265_1275delinsTGCTGAAAGTG (p.Val422=)
c.1262_1272delinsTGCTGAAAGTG (p.Val421=)
10g.119676820G>ACA471739432BAG3c.1266G>A (p.Val422=)
c.1263G>A (p.Val421=)
gnomAD v4
10g.119676820G>CCA5716525BAG3c.1266G>C (p.Val422=)
c.1263G>C (p.Val421=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119676820G=CA1940196716BAG3c.1266G= (p.Val422=)
c.1263G= (p.Val421=)
10g.119676820G>TCA471739431BAG3c.1266G>T (p.Val422=)
c.1263G>T (p.Val421=)
10g.119676821_119676830delCA204624BAG3c.1267_1276del (p.Leu423LysfsTer14)
c.1264_1273del (p.Leu422LysfsTer14)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119676821C>ACA378296948BAG3c.1267C>A (p.Leu423Met)
c.1264C>A (p.Leu422Met)
10g.119676821C>GCA378296949BAG3c.1267C>G (p.Leu423Val)
c.1264C>G (p.Leu422Val)
10g.119676821C>TCA471739434BAG3c.1267C>T (p.Leu423=)
c.1264C>T (p.Leu422=)
10g.119676822T>ACA378296950BAG3c.1268T>A (p.Leu423Gln)
c.1265T>A (p.Leu422Gln)
10g.119676822T>CCA378296951BAG3c.1268T>C (p.Leu423Pro)
c.1265T>C (p.Leu422Pro)
10g.119676822T>GCA378296952BAG3c.1268T>G (p.Leu423Arg)
c.1265T>G (p.Leu422Arg)
10g.119676823G>ACA471739437BAG3c.1269G>A (p.Leu423=)
c.1266G>A (p.Leu422=)
10g.119676823G>CCA471739438BAG3c.1269G>C (p.Leu423=)
c.1266G>C (p.Leu422=)
dbSNP
10g.119676823G=CA1940196717BAG3c.1269G= (p.Leu423=)
c.1266G= (p.Leu422=)
10g.119676823G>TCA471739439BAG3c.1269G>T (p.Leu423=)
c.1266G>T (p.Leu422=)
10g.119676824A>CCA378296953BAG3c.1270A>C (p.Lys424Gln)
c.1267A>C (p.Lys423Gln)
10g.119676824A>GCA378296954BAG3c.1270A>G (p.Lys424Glu)
c.1267A>G (p.Lys423Glu)
10g.119676824A>TCA378296955BAG3c.1270A>T (p.Lys424Ter)
c.1267A>T (p.Lys423Ter)
10g.119676825A>CCA378296956BAG3c.1271A>C (p.Lys424Thr)
c.1268A>C (p.Lys423Thr)
10g.119676825A>GCA378296957BAG3c.1271A>G (p.Lys424Arg)
c.1268A>G (p.Lys423Arg)
10g.119676825A>TCA378296958BAG3c.1271A>T (p.Lys424Ile)
c.1268A>T (p.Lys423Ile)
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=)

Number of alleles fetched