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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXW4
Single nucleotide variant
(synonymous variant +1 more)
Split hand-foot malformation 3
+2 more
GBenign
FBXW4
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GBenign/Likely benign
FBXW4
(R67W +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
FBXW4
(R262C +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
FBXW4, LOC130004563
Single nucleotide variant
(non-coding transcript variant +2 more)
not specified
+2 more
GBenign/Likely benign
FBXW4, LOC130004563
Microsatellite
(inframe_insertion +2 more)
Ectrodactyly
+1 more
GUncertain significance
FBXW4, LOC130004563
Microsatellite
(inframe_insertion +2 more)
not specified
+1 more
GConflicting classifications of pathogenicity
FBXW4, LOC130004563
(E167K)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
FBXW4, LOC130004563
(A158P)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GBenign
LOC130004563, FBXW4
(V154E)
Single nucleotide variant
(missense variant +2 more)
Split hand-foot malformation 3
+2 more
GBenign
FBXW4, LOC130004563
(G153R)
Single nucleotide variant
(missense variant +2 more)
FBXW4-related condition
+1 more
GConflicting classifications of pathogenicity
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