Gene dossier

FLCN

441 mutation records across 3 cancer labels and 3 source families.

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
FLCN p.X434_splice
splice
PLMESOLikely Driver1.2%cBioPortal, TCGA Pan-Cancer Atlas
FLCN p.S62R
substitution
ACCLikely Driver1.1%cBioPortal, TCGA Pan-Cancer Atlas
FLCN p.His429fs
duplication
UNSPECDriverNot reportedClinVar
FLCN p.His429fs
duplication
UNSPECDriverNot reportedClinVar
FLCN p.His429fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.His429fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Tyr463Ter
substitution
UNSPECDriverNot reportedClinVar
FLCN p.Tyr463Ter
substitution
UNSPECDriverNot reportedClinVar
FLCN p.Ile426fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Ile426fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Ser79Trp
substitution
UNSPECVUSNot reportedClinVar
FLCN p.Ser79Trp
substitution
UNSPECVUSNot reportedClinVar
FLCN p.Ala445Thr
substitution
UNSPECDriverNot reportedClinVar
FLCN p.Ala445Thr
substitution
UNSPECDriverNot reportedClinVar
FLCN p.Ser79fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Ser79fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Glu510_Trp511insTer
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Glu510_Trp511insTer
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Pro135fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Pro135fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Gln373Ter
substitution
UNSPECDriverNot reportedClinVar
FLCN p.Gln373Ter
substitution
UNSPECDriverNot reportedClinVar
FLCN p.Met394fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Met394fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Ile402fs
duplication
UNSPECDriverNot reportedClinVar
FLCN p.Ile402fs
duplication
UNSPECDriverNot reportedClinVar
FLCN p.Phe435fs
deletion
UNSPECDriverNot reportedClinVar
FLCN p.Phe435fs
deletion
UNSPECDriverNot reportedClinVar
FLCN c.1433-2A>G
substitution
UNSPECDriverNot reportedClinVar
FLCN c.1433-2A>G
substitution
UNSPECDriverNot reportedClinVar