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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TINF2
(L364fs +1 more)
Duplication
(frameshift variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
TINF2
(M326T +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TINF2
(T249K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TINF2
(R230* +1 more)
Single nucleotide variant
(nonsense)
Dyskeratosis congenita
+2 more
GConflicting classifications of pathogenicity
LOC130055403, TINF2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
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