Gene dossier

HNF1A

33 mutation records across 4 cancer labels and 4 source families.

0 actionable12 hotspotsNot reported
Top records

Prioritized variant evidence

Open in Explore
VariantCancerEvidenceFrequencySources
HNF1A p.D192Gfs*2
frameshift
CHRCCLikely Driver1.5%cBioPortal, TCGA Pan-Cancer Atlas
HNF1A p.R114H
substitution
BLCADriverHotspot0.24%cBioPortal, TCGA Pan-Cancer Atlas
HNF1A p.R114C
substitution
UCECDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
HNF1A p.R114H
substitution
UCECDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
HNF1A p.G288G
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.S591S
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.S591Y
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.I27L
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.R114C
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.R114H
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.R114L
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.G338A
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.G338G
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
HNF1A p.Gly292fs
duplication
UNSPECDriverNot reportedClinVar
HNF1A p.Gly292fs
duplication
UNSPECDriverNot reportedClinVar
HNF1A p.Ile27Leu
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Ile27Leu
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Gly31Asp
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Gly31Asp
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Ser574Gly
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Ser574Gly
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Leu389Val
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Leu389Val
substitution
UNSPECVUSNot reportedClinVar
HNF1A p.Arg171Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1A p.Arg171Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1A c.-4A>G
substitution
UNSPECDriverNot reportedClinVar
HNF1A c.-4A>G
substitution
UNSPECDriverNot reportedClinVar
HNF1A p.Pro379fs
deletion
UNSPECDriverNot reportedClinVar
HNF1A p.Pro379fs
deletion
UNSPECDriverNot reportedClinVar
HNF1A p.Gly47Arg
substitution
UNSPECVUSNot reportedClinVar