Gene dossier

AXIN2

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

0 actionable0 hotspotsNot reported
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Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
AXIN2 p.Glu706Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Glu706Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Gly665fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Gly665fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Arg656Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Arg656Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Trp663Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Trp663Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Ala684Val
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Ala684Val
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Pro245Ser
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Pro245Ser
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Met1fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Met1fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Thr693Met
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Thr693Met
substitution
UNSPECDriverNot reportedClinVar
AXIN2 c.1201-2A>G
substitution
UNSPECDriverNot reportedClinVar
AXIN2 c.1201-2A>G
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Gly546fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Gly546fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Pro65fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Pro65fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Tyr549fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Tyr549fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Glu548Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Glu548Ter
substitution
UNSPECDriverNot reportedClinVar
AXIN2 p.Phe770fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Phe770fs
deletion
UNSPECDriverNot reportedClinVar
AXIN2 p.Asn666fs
duplication
UNSPECDriverNot reportedClinVar
AXIN2 p.Asn666fs
duplication
UNSPECDriverNot reportedClinVar