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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLCN
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
FLCN
(A445T +1 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
FLCN
(R341Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
FLCN
(R320Q +1 more)
Single nucleotide variant
(missense variant)
FLCN-related condition
+5 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign
FLCN
(D198N +1 more)
Single nucleotide variant
(missense variant)
FLCN-related condition
+5 more
GConflicting classifications of pathogenicity
FLCN
(N184K +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
FLCN
(A90S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
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