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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SUFU
(R173K)
Single nucleotide variant
(missense variant)
not specified
Gnot provided
SUFU
(I291T)
Single nucleotide variant
(missense variant)
Gorlin syndrome
+3 more
GUncertain significance
SUFU
(A340S)
Single nucleotide variant
(missense variant)
Medulloblastoma
+5 more
GBenign/Likely benign
SUFU
(P341L)
Single nucleotide variant
(missense variant)
Gorlin syndrome
+2 more
GConflicting classifications of pathogenicity
SUFU
(R343H)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
SUFU
(S349G)
Single nucleotide variant
(missense variant)
Familial meningioma
+5 more
GConflicting classifications of pathogenicity
SUFU
(R362C)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
SUFU
(V369I)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
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