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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TK2
(Y109C +5 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
TK2
(Y117fs +5 more)
Deletion
(frameshift variant +1 more)
Mitochondrial DNA depletion syndrome, myopathic form
+2 more
GPathogenic/Likely pathogenic
TK2
(R116S +5 more)
Single nucleotide variant
(missense variant +1 more)
Mitochondrial DNA depletion syndrome, myopathic form
GLikely pathogenic
TK2
(Q125H +5 more)
Single nucleotide variant
(missense variant +1 more)
Mitochondrial DNA depletion syndrome, myopathic form
+1 more
GUncertain significance
TK2
(T108M +5 more)
Single nucleotide variant
(missense variant +1 more)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
+3 more
GPathogenic
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