BAG5 — 83 ClinVar variants
All ClinVar germline BAG5 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 60 flagged for review →
2 Pathogenic · 3 Likely pathogenic · 6 Likely benign · 72 Uncertain significance
Full BAG5 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 60
Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.
Predictors lean, ClinVar uncertain 33
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
BAG5 p.Ala184Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ala431Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ala72Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg235Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg271Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg285Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg287Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg390Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Asp231Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Asp248Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Cys166Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Cys420Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Gln73Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Glu237Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Glu323Gln
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Glu93Gln
Uncertain significance
Single submitter
cardiomyopathy, dilated, 2F
-
BAG5 p.Ile143Phe
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ile249Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ile28Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Leu203Phe
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Leu348Phe
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Leu384Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Leu407Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Lys108Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Lys290Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Met205Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Thr139Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Thr75Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Tyr113His
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Val245Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Val27Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Val369Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Val372Ile
Uncertain significance
Single submitter
Inborn genetic diseases
Predictors split 27
The independent predictors disagree with each other — read with care.
-
BAG5 p.Ala408Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg146Trp
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg329Gln
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg329Trp
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Arg77Cys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Asp57Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Gln311Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Gln415Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Glu192Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Glu362Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Glu74Gln
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Gly115Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Gly206Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Gly234Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.His274Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ile127Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ile130Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ile279Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ile64Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Leu310Phe
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Leu406Met
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Lys169Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Lys37Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Pro414Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Ser103Cys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Tyr150Cys
Uncertain significance
Single submitter
Inborn genetic diseases
-
BAG5 p.Val189Met
Uncertain significance
Single submitter
Inborn genetic diseases
All BAG5 variants
Pathogenic 2
- p.Arg197Ter No assertion criteria cardiomyopathy, dilated, 2F
- p.His7fs No assertion criteria cardiomyopathy, dilated, 2F
Likely pathogenic 3
- p.Arg390Ter Single submitter cardiomyopathy, dilated, 2F
- p.His136fs Single submitter cardiomyopathy, dilated, 2F
- p.Lys108fs No assertion criteria cardiomyopathy
Likely benign 6
- p.Asn210Ser Single submitter Inborn genetic diseases
- p.Ile28Val Single submitter Inborn genetic diseases
- p.Ile92Leu Single submitter Inborn genetic diseases
- p.Pro111= Single submitter
- p.Ser31Thr Single submitter
- p.Tyr255= Single submitter
Uncertain significance 72
- c.-12C>T Single submitter Inborn genetic diseases
- c.-28T>G Single submitter Inborn genetic diseases
- c.-29+612C>T Single submitter Inborn genetic diseases
- c.-29+617C>G Single submitter Inborn genetic diseases
- c.-29+636A>C Single submitter Inborn genetic diseases
- c.-29+654A>T Single submitter Inborn genetic diseases
- c.-29+670C>T Single submitter Inborn genetic diseases
- c.-29+693C>T Single submitter Inborn genetic diseases
- c.-29+694C>G Single submitter Inborn genetic diseases
- c.-5A>G Single submitter Inborn genetic diseases
- c.-6A>G Single submitter Inborn genetic diseases
- p.Ala184Thr Single submitter Inborn genetic diseases ⚠
- p.Ala408Val Single submitter Inborn genetic diseases ⚠
- p.Ala431Val Single submitter Inborn genetic diseases ⚠
- p.Ala72Val Single submitter Inborn genetic diseases ⚠
- p.Arg146Trp Single submitter Inborn genetic diseases ⚠
- p.Arg235Leu Single submitter Inborn genetic diseases ⚠
- p.Arg271Lys Single submitter Inborn genetic diseases ⚠
- p.Arg285Lys Single submitter Inborn genetic diseases ⚠
- p.Arg287Lys Single submitter Inborn genetic diseases ⚠
- p.Arg329Gln Single submitter Inborn genetic diseases ⚠
- p.Arg329Trp Single submitter Inborn genetic diseases ⚠
- p.Arg355fs Single submitter
- p.Arg390Gly Single submitter Inborn genetic diseases ⚠
- p.Arg77Cys Single submitter Inborn genetic diseases ⚠
- p.Asp231Asn Single submitter Inborn genetic diseases ⚠
- p.Asp248Asn Single submitter Inborn genetic diseases ⚠
- p.Asp57Val Single submitter Inborn genetic diseases ⚠
- p.Cys166Tyr Single submitter Inborn genetic diseases ⚠
- p.Cys420Arg Single submitter Inborn genetic diseases ⚠
- p.Gln311Arg Single submitter Inborn genetic diseases ⚠
- p.Gln415Arg Single submitter Inborn genetic diseases ⚠
- p.Gln73Arg Single submitter Inborn genetic diseases ⚠
- p.Glu192Lys Single submitter Inborn genetic diseases ⚠
- p.Glu237Asp Single submitter Inborn genetic diseases ⚠
- p.Glu323Gln Single submitter Inborn genetic diseases ⚠
- p.Glu362Gly Single submitter Inborn genetic diseases ⚠
- p.Glu74Gln Single submitter Inborn genetic diseases ⚠
- p.Glu93Gln Single submitter cardiomyopathy, dilated, 2F ⚠
- p.Gly115Arg Single submitter Inborn genetic diseases ⚠
- p.Gly206Ala Single submitter Inborn genetic diseases ⚠
- p.Gly234Ser Single submitter Inborn genetic diseases ⚠
- p.His274Tyr Single submitter Inborn genetic diseases ⚠
- p.Ile127Val Single submitter Inborn genetic diseases ⚠
- p.Ile130Thr Single submitter Inborn genetic diseases ⚠
- p.Ile143Phe Single submitter Inborn genetic diseases ⚠
- p.Ile249Thr Single submitter Inborn genetic diseases ⚠
- p.Ile279Thr Single submitter Inborn genetic diseases ⚠
- p.Ile28Thr Single submitter Inborn genetic diseases ⚠
- p.Ile64Thr Single submitter Inborn genetic diseases ⚠
- p.Leu203Phe Single submitter Inborn genetic diseases ⚠
- p.Leu310Phe Single submitter Inborn genetic diseases ⚠
- p.Leu348Phe Single submitter Inborn genetic diseases ⚠
- p.Leu384Ile Single submitter Inborn genetic diseases ⚠
- p.Leu406Met Single submitter Inborn genetic diseases ⚠
- p.Leu407Val Single submitter Inborn genetic diseases ⚠
- p.Lys108Glu Single submitter Inborn genetic diseases ⚠
- p.Lys169Thr Single submitter Inborn genetic diseases ⚠
- p.Lys290Glu Single submitter Inborn genetic diseases ⚠
- p.Lys37Thr Single submitter Inborn genetic diseases ⚠
- p.Met205Ile Single submitter Inborn genetic diseases ⚠
- p.Pro414Leu Single submitter Inborn genetic diseases ⚠
- p.Ser103Cys Single submitter Inborn genetic diseases ⚠
- p.Thr139Ile Single submitter Inborn genetic diseases ⚠
- p.Thr75Ala Single submitter Inborn genetic diseases ⚠
- p.Tyr113His Single submitter Inborn genetic diseases ⚠
- p.Tyr150Cys Single submitter Inborn genetic diseases ⚠
- p.Val189Met Single submitter Inborn genetic diseases ⚠
- p.Val245Ala Single submitter Inborn genetic diseases ⚠
- p.Val27Gly Single submitter Inborn genetic diseases ⚠
- p.Val369Ile Single submitter Inborn genetic diseases ⚠
- p.Val372Ile Single submitter Inborn genetic diseases ⚠