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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PXDN
(R880C)
Single nucleotide variant
(missense variant)
Anterior segment dysgenesis 7
GPathogenic
PXDN
(C857fs)
Deletion
(frameshift variant)
Anterior segment dysgenesis 7
GPathogenic
PXDN
(L792fs)
Deletion
(frameshift variant)
Anterior segment dysgenesis 7
GPathogenic
PXDN
(R341*)
Single nucleotide variant
(nonsense)
Anterior segment dysgenesis 7
GPathogenic
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