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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AKT3
(R465W)
Single nucleotide variant
(missense variant +1 more)
not provided
+9 more
GPathogenic/Likely pathogenic
OLikely oncogenic
AKT3
(Y414C)
Single nucleotide variant
(missense variant)
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2
GUncertain significance