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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TUBGCP6
(N1613fs)
Duplication
(frameshift variant)
Microcephaly and chorioretinopathy 1
GLikely pathogenic
TUBGCP6
(Q1303*)
Single nucleotide variant
(nonsense)
Microcephaly and chorioretinopathy 1
GLikely pathogenic
TUBGCP6
(S852L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TUBGCP6
(W539fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
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