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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BAG3
(N16D)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
BAG3
(P23S)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
BAG3
(P209S)
Single nucleotide variant
(missense variant)
Myofibrillar myopathy 6
+4 more
GPathogenic/Likely pathogenic
BAG3
(Y233C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
BAG3
(T242A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1HH
+3 more
GUncertain significance
BAG3
(H248R)
Single nucleotide variant
(missense variant)
Myofibrillar myopathy 6
+4 more
GUncertain significance
BAG3
(A262V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
BAG3
(V298M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
BAG3
(V328A)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
BAG3
(E363A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
BAG3
(P384S)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1HH
+2 more
GConflicting classifications of pathogenicity
BAG3
Duplication
(inframe_insertion)
not provided
+2 more
GUncertain significance
BAG3
(A405V)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
BAG3
(E471Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
BAG3
(G483S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
BAG3
(P502A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
BAG3
(P575L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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