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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BCL11B
(E749fs +3 more)
Duplication
(frameshift variant)
Immunodeficiency 49
+1 more
GPathogenic
BCL11B
(A511V +3 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities
GUncertain significance
BCL11B
(K353fs +3 more)
Deletion
(frameshift variant)
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities
GPathogenic
BCL11B
(C60F +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities
GUncertain significance
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