Gene dossier

EXT1

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

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
EXT1 p.Arg340Leu
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Arg340Leu
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Lys177fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Lys177fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Arg340Cys
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Arg340Cys
substitution
UNSPECDriverNot reportedClinVar
EXT1 c.962+3_962+6del
Microsatellite
UNSPECDriverNot reportedClinVar
EXT1 c.962+3_962+6del
Microsatellite
UNSPECDriverNot reportedClinVar
EXT1 p.Leu490fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Leu490fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Leu490fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Leu490fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Leu181fs
Microsatellite
UNSPECDriverNot reportedClinVar
EXT1 p.Leu181fs
Microsatellite
UNSPECDriverNot reportedClinVar
EXT1 p.Leu490fs
duplication
UNSPECDriverNot reportedClinVar
EXT1 p.Leu490fs
duplication
UNSPECDriverNot reportedClinVar
EXT1 c.1884-1G>C
substitution
UNSPECDriverNot reportedClinVar
EXT1 c.1884-1G>C
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Ser478fs
duplication
UNSPECDriverNot reportedClinVar
EXT1 p.Ser478fs
duplication
UNSPECDriverNot reportedClinVar
EXT1 c.1884-1G>A
substitution
UNSPECDriverNot reportedClinVar
EXT1 c.1884-1G>A
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Gln2Ter
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Gln2Ter
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Ala693fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Ala693fs
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Trp517Ter
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Trp517Ter
substitution
UNSPECDriverNot reportedClinVar
EXT1 p.Phe250_Leu251insTer
deletion
UNSPECDriverNot reportedClinVar
EXT1 p.Phe250_Leu251insTer
deletion
UNSPECDriverNot reportedClinVar