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Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HDAC4
Single nucleotide variant
(synonymous variant)
HDAC4-related condition
+1 more
GConflicting classifications of pathogenicity
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
HDAC4
(S807G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HDAC4
(A786T +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
HDAC4
Duplication
(intron variant)
not provided
GUncertain significance
HDAC4
Single nucleotide variant
(synonymous variant)
HDAC4-related condition
+1 more
GConflicting classifications of pathogenicity
HDAC4
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
HDAC4
(K664R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
HDAC4
Single nucleotide variant
(intron variant)
not specified
GLikely benign
HDAC4
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
HDAC4
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
HDAC4
(P545L +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with central hypotonia and dysmorphic facies
+2 more
GUncertain significance
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
HDAC4
(R448Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
HDAC4
(T367M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HDAC4
Single nucleotide variant
(intron variant)
HDAC4-related condition
+2 more
GBenign/Likely benign
HDAC4
(V320I)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
HDAC4
(A319T)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
HDAC4
(P318S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
HDAC4
(G308R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HDAC4
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
HDAC4
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
HDAC4
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
HDAC4
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
HDAC4
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
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