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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRRAP
(H152R)
Single nucleotide variant
(missense variant)
Developmental delay with or without dysmorphic facies and autism
GUncertain significance
TRRAP
(S886I)
Single nucleotide variant
(missense variant)
Developmental delay with or without dysmorphic facies and autism
GUncertain significance
TRRAP
(H1879R +2 more)
Single nucleotide variant
(missense variant)
Developmental delay with or without dysmorphic facies and autism
GUncertain significance
TRRAP
(T2689S +2 more)
Single nucleotide variant
(missense variant)
Developmental delay with or without dysmorphic facies and autism
+1 more
GUncertain significance
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