Gene dossier

NTHL1

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

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
NTHL1 c.685+1G>A
substitution
UNSPECDriverNot reportedClinVar
NTHL1 c.685+1G>A
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Glu265fs
deletion
UNSPECDriverNot reportedClinVar
NTHL1 p.Glu265fs
deletion
UNSPECDriverNot reportedClinVar
NTHL1 p.Ala71fs
duplication
UNSPECDriverNot reportedClinVar
NTHL1 p.Ala71fs
duplication
UNSPECDriverNot reportedClinVar
NTHL1 p.Gly68fs
deletion
UNSPECDriverNot reportedClinVar
NTHL1 p.Gly68fs
deletion
UNSPECDriverNot reportedClinVar
NTHL1 p.Gln279Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Gln279Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Trp261Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Trp261Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Glu202Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Glu202Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Gln158Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Gln158Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Asp154fs
deletion
UNSPECDriverNot reportedClinVar
NTHL1 p.Asp154fs
deletion
UNSPECDriverNot reportedClinVar
NTHL1 p.Arg145Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Arg145Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Gln137Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Gln137Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Ser131fs
Microsatellite
UNSPECDriverNot reportedClinVar
NTHL1 p.Ser131fs
Microsatellite
UNSPECDriverNot reportedClinVar
NTHL1 p.Tyr122Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Tyr122Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Tyr122Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Tyr122Ter
substitution
UNSPECDriverNot reportedClinVar
NTHL1 p.Arg121fs
duplication
UNSPECDriverNot reportedClinVar
NTHL1 p.Arg121fs
duplication
UNSPECDriverNot reportedClinVar