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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS35
(E787K)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(L774M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
VPS35
(A737V)
Single nucleotide variant
(missense variant)
Parkinson disease 17
GUncertain significance
VPS35
(D620N)
Single nucleotide variant
(missense variant)
Parkinson disease 17
GPathogenic
VPS35
(M607V)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(H599R)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(I560T)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(R524W)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(Y507F)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(P316S)
Single nucleotide variant
(missense variant)
Parkinson disease 17
GUncertain significance
VPS35
(I241M)
Single nucleotide variant
(missense variant)
Parkinson disease 17
Gnot provided
VPS35
(M57I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
VPS35
(G51S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
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