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Items: 42

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APPL2
(E663Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(E620K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(D650N +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
APPL2
(Q576H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(I616T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(I615L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(H527Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(V526L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(A473V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(R454Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(L447W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
APPL2
(F480L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(R427C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(T416K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(P452L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(A451V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(A451T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(E447G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(S410T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(T359I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(L347F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(G352R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(T303M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(D294E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(N327D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(N308T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(E216D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(E265Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(F216L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(I201L +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
APPL2
(S134P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(A168G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(E168D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(N138K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(A136T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(R76Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(H44R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(Y48C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(R46H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
APPL2
(D35H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
APPL2
(V25M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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