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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PNKP
(A440fs)
Duplication
(frameshift variant)
Microcephaly, seizures, and developmental delay
GLikely pathogenic
PNKP
Single nucleotide variant
(splice donor variant)
Inborn genetic diseases
+2 more
GLikely pathogenic
PNKP
(R259W)
Single nucleotide variant
(missense variant)
Microcephaly, seizures, and developmental delay
+1 more
GUncertain significance
PNKP
(P119Q)
Single nucleotide variant
(missense variant)
Microcephaly, seizures, and developmental delay
GUncertain significance
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