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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSEN2
(V108F)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
TSEN2
(K130T)
Single nucleotide variant
(missense variant +1 more)
Pontoneocerebellar hypoplasia
+3 more
GBenign/Likely benign
TSEN2
(N144S)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
TSEN2
(P218L)
Single nucleotide variant
(missense variant +2 more)
Pontocerebellar hypoplasia type 2B
GUncertain significance
TSEN2
(T279R +2 more)
Single nucleotide variant
(missense variant +1 more)
Pontoneocerebellar hypoplasia
+2 more
GConflicting classifications of pathogenicity
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