Gene dossier

GPC3

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

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
GPC3 c.1292+1G>T
substitution
UNSPECDriverNot reportedClinVar
GPC3 c.1292+1G>T
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.Arg199Ter
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.Arg199Ter
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.His121Tyr
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.His121Tyr
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.Ala569Thr
substitution
UNSPECVUSNot reportedClinVar
GPC3 p.Ala569Thr
substitution
UNSPECVUSNot reportedClinVar
GPC3 p.Arg387Ter
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.Arg387Ter
substitution
UNSPECDriverNot reportedClinVar
GPC3 c.1574-?_*379+?del
deletion
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:417449
deletion
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:476637
duplication
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:476637|UNSPEC
duplication
UNSPECDriverNot reportedClinVar
GPC3 p.Asn210fs
deletion
UNSPECDriverNot reportedClinVar
GPC3 p.Asn210fs
deletion
UNSPECDriverNot reportedClinVar
GPC3 p.Glu491Ter
substitution
UNSPECDriverNot reportedClinVar
GPC3 p.Glu491Ter
substitution
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:583690
deletion
UNSPECDriverNot reportedClinVar
GPC3 p.Ala436fs
deletion
UNSPECDriverNot reportedClinVar
GPC3 p.Ala436fs
deletion
UNSPECDriverNot reportedClinVar
GPC3 p.Asp172Ter
duplication
UNSPECDriverNot reportedClinVar
GPC3 p.Asp172Ter
duplication
UNSPECDriverNot reportedClinVar
GPC3 p.Pro28fs
duplication
UNSPECDriverNot reportedClinVar
GPC3 p.Pro28fs
duplication
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:662850
duplication
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:662850|UNSPEC
duplication
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:832421
deletion
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:830889
deletion
UNSPECDriverNot reportedClinVar
GPC3 ClinVar:830784
deletion
UNSPECDriverNot reportedClinVar