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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS45
(T39A +1 more)
Single nucleotide variant
(missense variant +1 more)
Congenital neutropenia-myelofibrosis-nephromegaly syndrome
GUncertain significance
VPS45
(N104S +1 more)
Single nucleotide variant
(missense variant +1 more)
Congenital neutropenia-myelofibrosis-nephromegaly syndrome
GUncertain significance
VPS45
(E189G +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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