Gene dossier

PRKN

36 mutation records across 1 cancer labels and 1 source families.

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
PRKN c.(?_171+24726
deletion
UNSPECDriverNot reportedClinVar
PRKN c.(8_8
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Arg275Trp
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Arg275Trp
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Lys211Asn
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Lys211Asn
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Thr240Met
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Thr240Met
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Gly430Asp
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Gly430Asp
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Asn52fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Asn52fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Arg33Gln
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Arg33Gln
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Cys253Tyr
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Cys253Tyr
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Gln34fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Gln34fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Leu331fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Leu331fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Trp74fs
duplication
UNSPECDriverNot reportedClinVar
PRKN p.Trp74fs
duplication
UNSPECDriverNot reportedClinVar
PRKN p.Pro113fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Pro113fs
deletion
UNSPECDriverNot reportedClinVar
PRKN p.Cys441Arg
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Cys441Arg
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Gln25Ter
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Gln25Ter
substitution
UNSPECDriverNot reportedClinVar
PRKN p.Cys201Ter
insertion
UNSPECDriverNot reportedClinVar
PRKN p.Cys201Ter
insertion
UNSPECDriverNot reportedClinVar