Gene dossier

MSH6

3,844 mutation records across 1 cancer labels and 1 source families.

0 actionable0 hotspotsDNA Repair
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
MSH6 p.Lys218Ter
duplication
UNSPECDriverNot reportedClinVar
MSH6 p.Lys218Ter
duplication
UNSPECDriverNot reportedClinVar
MSH6 p.Val1212fs
duplication
UNSPECDriverNot reportedClinVar
MSH6 p.Val1212fs
duplication
UNSPECDriverNot reportedClinVar
MSH6 p.Lys1233fs
deletion
UNSPECDriverNot reportedClinVar
MSH6 p.Lys1233fs
deletion
UNSPECDriverNot reportedClinVar
MSH6 c.3173-1G>C
substitution
UNSPECDriverNot reportedClinVar
MSH6 c.3173-1G>C
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Arg1331Ter
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Arg1331Ter
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Leu370Ser
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Leu370Ser
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Arg378_Arg379insTer
Microsatellite
UNSPECDriverNot reportedClinVar
MSH6 p.Arg378_Arg379insTer
Microsatellite
UNSPECDriverNot reportedClinVar
MSH6 p.Asp380fs
deletion
UNSPECDriverNot reportedClinVar
MSH6 p.Asp380fs
deletion
UNSPECDriverNot reportedClinVar
MSH6 p.Arg385del
Microsatellite
UNSPECDriverNot reportedClinVar
MSH6 p.Arg385del
Microsatellite
UNSPECDriverNot reportedClinVar
MSH6 p.Tyr397fs
deletion
UNSPECDriverNot reportedClinVar
MSH6 p.Tyr397fs
deletion
UNSPECDriverNot reportedClinVar
MSH6 p.Leu435Pro
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Leu435Pro
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Leu449Pro
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Leu449Pro
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Gln475fs
duplication
UNSPECDriverNot reportedClinVar
MSH6 p.Gln475fs
duplication
UNSPECDriverNot reportedClinVar
MSH6 p.Arg482Ter
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Arg482Ter
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Glu493Ter
substitution
UNSPECDriverNot reportedClinVar
MSH6 p.Glu493Ter
substitution
UNSPECDriverNot reportedClinVar