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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASP10
(L285F +2 more)
Single nucleotide variant
(missense variant +1 more)
Autoimmune lymphoproliferative syndrome type 2A
GUncertain significance
CASP10
(I406L +2 more)
Single nucleotide variant
(missense variant +1 more)
Hypomyelination and Congenital Cataract
+2 more
GConflicting classifications of pathogenicity
CASP10
(V410I +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign
CASP10
(Y446C +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign
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