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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTUD6B
Single nucleotide variant
(5 prime UTR variant)
not specified
+2 more
GConflicting classifications of pathogenicity
OTUD6B
Single nucleotide variant
(5 prime UTR variant)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GUncertain significance
OTUD6B
Single nucleotide variant
(splice acceptor variant)
Intellectual disability
+2 more
GPathogenic
OTUD6B
(R14* +1 more)
Single nucleotide variant
(nonsense)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
+5 more
GPathogenic
OTUD6B
(L127fs +1 more)
Deletion
(frameshift variant)
Intellectual disability
+2 more
GPathogenic
OTUD6B
(A130D +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
OTUD6B
(Y85C +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability
+2 more
GLikely pathogenic
OTUD6B
(E110* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
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