Gene dossier

LRP5

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

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
LRP5 p.Trp10Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Trp10Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Arg428Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Arg428Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Asp490fs
deletion
UNSPECDriverNot reportedClinVar
LRP5 p.Asp490fs
deletion
UNSPECDriverNot reportedClinVar
LRP5 p.Asp718Ter
duplication
UNSPECDriverNot reportedClinVar
LRP5 p.Asp718Ter
duplication
UNSPECDriverNot reportedClinVar
LRP5 p.Gln853Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Gln853Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Glu1270fs
deletion
UNSPECDriverNot reportedClinVar
LRP5 p.Glu1270fs
deletion
UNSPECDriverNot reportedClinVar
LRP5 p.Arg494Gln
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Arg494Gln
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Arg570Trp
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Arg570Trp
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Val667Met
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Val667Met
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Glu485Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Glu485Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Trp734Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Trp734Ter
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Asp769fs
deletion
UNSPECDriverNot reportedClinVar
LRP5 p.Asp769fs
deletion
UNSPECDriverNot reportedClinVar
LRP5 c.4488+2T>G
substitution
UNSPECDriverNot reportedClinVar
LRP5 c.4488+2T>G
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Leu145Phe
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Leu145Phe
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Thr552Met
substitution
UNSPECDriverNot reportedClinVar
LRP5 p.Thr552Met
substitution
UNSPECDriverNot reportedClinVar