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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDC42BPB
(H1695fs)
Duplication
(frameshift variant)
not specified
GUncertain significance
CDC42BPB
Single nucleotide variant
(intron variant)
not specified
GLikely benign
CDC42BPB
Single nucleotide variant
(intron variant)
not specified
GUncertain significance
CDC42BPB
(D513E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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