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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBCK
(R744P +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TBCK
Single nucleotide variant
(intron variant)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
+1 more
GBenign
TBCK
(R126*)
Single nucleotide variant
(nonsense +2 more)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
+2 more
GPathogenic
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