Gene dossier

AIP

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

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

Open in Explore
VariantCancerEvidenceFrequencySources
AIP p.Gln14Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln14Ter
substitution
UNSPECDriverNot reportedClinVar
AIP c.469-1G>A
substitution
UNSPECVUSNot reportedClinVar
AIP c.469-1G>A
substitution
UNSPECVUSNot reportedClinVar
AIP p.Arg304Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg304Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg304Gln
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg304Gln
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg81Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg81Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln142Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln142Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln164Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln164Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln217Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Gln217Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Cys238Tyr
substitution
UNSPECDriverNot reportedClinVar
AIP p.Cys238Tyr
substitution
UNSPECDriverNot reportedClinVar
AIP p.Phe269_His275dup
duplication
UNSPECDriverNot reportedClinVar
AIP p.Phe269_His275dup
duplication
UNSPECDriverNot reportedClinVar
AIP p.Arg271Trp
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg271Trp
substitution
UNSPECDriverNot reportedClinVar
AIP p.Arg307fs
duplication
UNSPECDriverNot reportedClinVar
AIP p.Arg307fs
duplication
UNSPECDriverNot reportedClinVar
AIP p.Glu116_Val124del
deletion
UNSPECDriverNot reportedClinVar
AIP p.Glu116_Val124del
deletion
UNSPECDriverNot reportedClinVar
AIP p.Trp73Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Trp73Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Lys215Ter
substitution
UNSPECDriverNot reportedClinVar
AIP p.Lys215Ter
substitution
UNSPECDriverNot reportedClinVar