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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPK1
(D101V +4 more)
Single nucleotide variant
(missense variant +2 more)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
+1 more
GUncertain significance
TPK1
(T149I +4 more)
Single nucleotide variant
(missense variant +1 more)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
GUncertain significance
TPK1
(L123F +3 more)
Single nucleotide variant
(missense variant +2 more)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
GConflicting classifications of pathogenicity
TPK1
(P7L)
Single nucleotide variant
(missense variant +3 more)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
+1 more
GUncertain significance
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