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Items: 44

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130003576, WAC
(G20E)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC130003576, WAC
(Y25C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(R42K)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(E88fs +1 more)
Microsatellite
(frameshift variant)
Inborn genetic diseases
+1 more
GPathogenic
WAC
Deletion
(splice acceptor variant)
Inborn genetic diseases
GUncertain significance
WAC
(S56T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(H57fs +1 more)
Duplication
(frameshift variant)
Inborn genetic diseases
GPathogenic
WAC
(S105I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(S125* +1 more)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
GPathogenic
WAC
(W112R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
WAC
(S135N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(T150A +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
WAC
(S169G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GLikely benign
WAC
(L170M +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(S177Y +1 more)
Single nucleotide variant
(missense variant +1 more)
DeSanto-Shinawi syndrome due to WAC point mutation
+2 more
GUncertain significance
WAC
(A237V +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(T244P +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
WAC
(H210D +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(T214S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(S220P +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(T269S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(T224M +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
WAC
(H274N +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WAC
(S205T +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(L318del +2 more)
Microsatellite
(inframe_deletion)
Inborn genetic diseases
GUncertain significance
WAC
(L264V +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(Q330R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(V278M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
WAC
(P419L +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
WAC
(S425G +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WAC
(P438L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(Q442P +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
WAC
(K458R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(T496P +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(V439I +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
WAC
(N501S +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WAC
(T507M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(C553Y +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
(P557A +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
WAC
(K478R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WAC
Single nucleotide variant
(intron variant)
Inborn genetic diseases
GLikely benign
WAC
(R519Q +2 more)
Single nucleotide variant
(missense variant)
DeSanto-Shinawi syndrome due to WAC point mutation
+1 more
GUncertain significance
WAC
(Q587* +2 more)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
GUncertain significance
WAC
(V602M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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