Gene dossier

MSH3

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

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
MSH3 p.Lys383fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Lys383fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Tyr921fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Tyr921fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 c.2319-1G>A
substitution
UNSPECDriverNot reportedClinVar
MSH3 c.2319-1G>A
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Gln949Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Gln949Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Pro49fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Pro49fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Gln106Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Gln106Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Glu154fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Glu154fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Gln192Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Gln192Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Thr196fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Thr196fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Glu233Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Glu233Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Arg268Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Arg268Ter
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Val292fs
Microsatellite
UNSPECDriverNot reportedClinVar
MSH3 p.Val292fs
Microsatellite
UNSPECDriverNot reportedClinVar
MSH3 p.Lys303Asn
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Lys303Asn
substitution
UNSPECDriverNot reportedClinVar
MSH3 p.Phe326fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Phe326fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Leu347fs
deletion
UNSPECDriverNot reportedClinVar
MSH3 p.Leu347fs
deletion
UNSPECDriverNot reportedClinVar