Gene dossier

NBN

545 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
NBN p.Lys219fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Lys219fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Leu281fs
duplication
UNSPECDriverNot reportedClinVar
NBN p.Leu281fs
duplication
UNSPECDriverNot reportedClinVar
NBN p.Gln326Ter
substitution
UNSPECDriverNot reportedClinVar
NBN p.Gln326Ter
substitution
UNSPECDriverNot reportedClinVar
NBN p.Ile171Val
substitution
UNSPECDriverNot reportedClinVar
NBN p.Ile171Val
substitution
UNSPECDriverNot reportedClinVar
NBN p.Arg215Trp
substitution
UNSPECDriverNot reportedClinVar
NBN p.Arg215Trp
substitution
UNSPECDriverNot reportedClinVar
NBN p.Glu248fs
duplication
UNSPECDriverNot reportedClinVar
NBN p.Glu248fs
duplication
UNSPECDriverNot reportedClinVar
NBN p.Lys233fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Lys233fs
deletion
UNSPECDriverNot reportedClinVar
NBN c.321-2A>G
substitution
UNSPECDriverNot reportedClinVar
NBN c.321-2A>G
substitution
UNSPECDriverNot reportedClinVar
NBN p.Phe102fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Phe102fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Asn30fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Asn30fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Ser42fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Ser42fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Pro381fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Pro381fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Gln492Ter
substitution
UNSPECDriverNot reportedClinVar
NBN p.Gln492Ter
substitution
UNSPECDriverNot reportedClinVar
NBN p.Asp61fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Asp61fs
deletion
UNSPECDriverNot reportedClinVar
NBN p.Arg43Ter
substitution
UNSPECDriverNot reportedClinVar
NBN p.Arg43Ter
substitution
UNSPECDriverNot reportedClinVar