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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBR1
(G58V)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
TBR1
(S194F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBR1
(S238fs)
Deletion
(frameshift variant)
Moderate global developmental delay
+2 more
GPathogenic/Likely pathogenic
TBR1
(T457fs)
Indel
(frameshift variant)
Intellectual disability
+2 more
GPathogenic/Likely pathogenic
TBR1
(Q552fs)
Deletion
(frameshift variant)
Intellectual disability
+2 more
GLikely pathogenic
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