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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNPO2
Single nucleotide variant
(splice donor variant)
Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
GLikely pathogenic
TNPO2
(Y515H)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
GUncertain significance
TNPO2
(P514S)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
GUncertain significance
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