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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRAPPC9
(R1148Q +5 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual Disability, Recessive
+5 more
GConflicting classifications of pathogenicity
TRAPPC9
(A438V +3 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 13
+3 more
GUncertain significance
TRAPPC9
(Q272K +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GUncertain significance
TRAPPC9
(R47Q)
Single nucleotide variant
(missense variant +1 more)
Intellectual Disability, Recessive
+4 more
GUncertain significance
TRAPPC9
(M7V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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