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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EXOSC3
(D132A)
Single nucleotide variant
(missense variant)
Hypotonia
+5 more
GPathogenic
EXOSC3
(I128fs)
Duplication
(frameshift variant)
Pontocerebellar hypoplasia type 1B
GPathogenic
EXOSC3
(G70D)
Single nucleotide variant
(missense variant)
Pontocerebellar hypoplasia type 1B
GUncertain significance
EXOSC3
(G31A)
Single nucleotide variant
(missense variant)
Abnormal cerebellum morphology
+8 more
GPathogenic/Likely pathogenic
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