Gene dossier

AR

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

0 actionable9 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
AR p.E308K
substitution
CHOLLikely Driver2.8%cBioPortal, TCGA Pan-Cancer Atlas
AR p.A597T
substitution
DLBCLNOSLikely Driver2.4%cBioPortal, TCGA Pan-Cancer Atlas
AR p.V758L
substitution
DLBCLNOSLikely Driver2.4%cBioPortal, TCGA Pan-Cancer Atlas
AR p.H875Y
substitution
COADREADDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
AR p.L702H
substitution
COADREADDriverHotspot0.19%cBioPortal, TCGA Pan-Cancer Atlas
AR p.L702H
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.L702L
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.T878A
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.T878S
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.H875Y
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.W742C
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.W742L
substitution
Not reportedDriverHotspotNot reportedCancer Hotspots
AR p.Val867Met
substitution
UNSPECDriverNot reportedClinVar
AR p.Val867Met
substitution
UNSPECDriverNot reportedClinVar
AR p.Ser648Asn
substitution
UNSPECDriverNot reportedClinVar
AR p.Ser648Asn
substitution
UNSPECDriverNot reportedClinVar
AR p.Val731Met
substitution
UNSPECDriverNot reportedClinVar
AR p.Val731Met
substitution
UNSPECDriverNot reportedClinVar
AR p.Arg609Lys
substitution
UNSPECDriverNot reportedClinVar
AR p.Arg609Lys
substitution
UNSPECDriverNot reportedClinVar
AR p.Thr878Ala
substitution
UNSPECDriverNot reportedClinVar
AR p.Thr878Ala
substitution
UNSPECDriverNot reportedClinVar
AR p.Thr878Ser
substitution
UNSPECDriverNot reportedClinVar
AR p.Thr878Ser
substitution
UNSPECDriverNot reportedClinVar
AR p.His875Tyr
substitution
UNSPECDriverNot reportedClinVar
AR p.His875Tyr
substitution
UNSPECDriverNot reportedClinVar
AR p.Gln903Arg
substitution
UNSPECDriverNot reportedClinVar
AR p.Gln903Arg
substitution
UNSPECDriverNot reportedClinVar
AR p.Ala722Thr
substitution
UNSPECVUSNot reportedClinVar
AR p.Ala722Thr
substitution
UNSPECVUSNot reportedClinVar