Gene dossier

SMARCB1

108 mutation records across 10 cancer labels and 4 source families.

0 actionable15 hotspotsChromatin
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
SMARCB1 p.T325P
substitution
DLBCLNOSLikely Driver2.4%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.K364R
substitution
CHRCCLikely Driver1.5%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.T381M
substitution
CHRCCLikely Driver1.5%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.E95K
substitution
PLMESOLikely Driver1.2%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R374W
substitution
PAADDriverHotspot0.56%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.K364del
deletion
STADDriverHotspot0.46%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R377H
substitution
STADDriverHotspot0.46%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R374W
substitution
UCECDriverHotspot0.39%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R374Q
substitution
PRCCDriverHotspot0.36%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R377C
substitution
DIFGDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R377H
substitution
COADREADDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R377C
substitution
COADREADDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R374Q
substitution
COADREADDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
SMARCB1 p.R377C
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
SMARCB1 p.R377H
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
SMARCB1 p.R377L
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
SMARCB1 p.R374Q
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
SMARCB1 p.R374W
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
SMARCB1 p.K364del
inframe
Not reportedDriverHotspotNot reportedCancer Hotspots
SMARCB1 p.Gln318fs
deletion
UNSPECDriverNot reportedClinVar
SMARCB1 p.Gln318fs
deletion
UNSPECDriverNot reportedClinVar
SMARCB1 ClinVar:8023
deletion
UNSPECDriverNot reportedClinVar
SMARCB1 p.Gln198fs
deletion
UNSPECDriverNot reportedClinVar
SMARCB1 p.Gln198fs
deletion
UNSPECDriverNot reportedClinVar
SMARCB1 c.986+1G>A
substitution
UNSPECDriverNot reportedClinVar
SMARCB1 c.986+1G>A
substitution
UNSPECDriverNot reportedClinVar
SMARCB1 p.Gln12Ter
substitution
UNSPECDriverNot reportedClinVar
SMARCB1 p.Gln12Ter
substitution
UNSPECDriverNot reportedClinVar
SMARCB1 c.629-361_795+2103dup
duplication
UNSPECDriverNot reportedClinVar
SMARCB1 c.629-361_795+2103dup
duplication
UNSPECDriverNot reportedClinVar