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Links from Gene

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TWNK
(T276M)
Single nucleotide variant
(missense variant +2 more)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
GUncertain significance
TWNK
(P211S)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
TWNK
(A504V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TWNK
(I367M)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
TWNK
(F100C)
Single nucleotide variant
(missense variant +2 more)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
GUncertain significance
TWNK
(T547A +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TWNK
(R374G)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
TWNK
(I367V)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
TWNK
(R334*)
Single nucleotide variant
(nonsense +2 more)
See cases
GLikely pathogenic
TWNK
(A359fs)
Deletion
(frameshift variant +2 more)
See cases
GUncertain significance
TWNK
(R329*)
Single nucleotide variant
(nonsense +2 more)
not provided
GPathogenic
TWNK
Copy number gain
See cases
GUncertain significance
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