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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXW11
(R460C +6 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
FBXW11
(P442A +6 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental, jaw, eye, and digital syndrome
GUncertain significance
FBXW11
(H245fs +6 more)
Duplication
(frameshift variant)
Neurodevelopmental, jaw, eye, and digital syndrome
GUncertain significance
FBXW11
(R122* +6 more)
Single nucleotide variant
(nonsense)
Neurodevelopmental, jaw, eye, and digital syndrome
GUncertain significance
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