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Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLCN
(Q533* +1 more)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
FLCN
Microsatellite
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
FLCN
(W511* +1 more)
Single nucleotide variant
(nonsense)
not provided
+6 more
GPathogenic
FLCN
(K508del +1 more)
Deletion
(inframe_deletion)
FLCN-related condition
+3 more
GPathogenic/Likely pathogenic
FLCN
Single nucleotide variant
(splice acceptor variant)
not provided
+2 more
GPathogenic/Likely pathogenic
FLCN
(F435fs +1 more)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic
FLCN
(H447fs +1 more)
Duplication
(frameshift variant)
Nonpapillary renal cell carcinoma
+7 more
GPathogenic
FLCN
(H447fs +1 more)
Deletion
(frameshift variant)
Nonpapillary renal cell carcinoma
+7 more
GPathogenic
FLCN
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
FLCN
(I402fs +1 more)
Duplication
(frameshift variant)
not provided
+2 more
GPathogenic
FLCN
(V400F +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
FLCN
(M394fs +1 more)
Deletion
(frameshift variant)
not provided
+2 more
GPathogenic
FLCN
Single nucleotide variant
(intron variant)
Birt-Hogg-Dube syndrome
+7 more
GBenign/Likely benign
FLCN
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
FLCN
(Q373* +1 more)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
FLCN
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
FLCN
(Q354* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
FLCN
(G319fs +1 more)
Duplication
(frameshift variant)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic
FLCN
(E315fs +1 more)
Deletion
(frameshift variant)
FLCN-related condition
+3 more
GPathogenic
FLCN
Single nucleotide variant
(intron variant)
Birt-Hogg-Dube syndrome
+4 more
GBenign
FLCN
(A277fs +1 more)
Duplication
(frameshift variant)
Birt-Hogg-Dube syndrome
GPathogenic
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign
FLCN
(A204* +1 more)
Indel
(nonsense)
not provided
+1 more
GPathogenic
FLCN
Single nucleotide variant
(intron variant)
not provided
+4 more
GBenign
FLCN
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
FLCN
(Q116*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
FLCN
(V107fs)
Indel
(frameshift variant)
not provided
+2 more
GPathogenic
FLCN
(D99fs)
Deletion
(frameshift variant)
not provided
+2 more
GPathogenic
FLCN
Single nucleotide variant
(splice acceptor variant)
not provided
+7 more
GPathogenic/Likely pathogenic
FLCN
(L29fs)
Duplication
(frameshift variant)
not provided
GPathogenic
FLCN
(R17P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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