Gene dossier

HNF1B

80 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
HNF1B p.Arg177Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg177Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg276Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg276Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Ser465Arg
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Ser465Arg
substitution
UNSPECDriverNot reportedClinVar
HNF1B c.544+1G>A
substitution
UNSPECDriverNot reportedClinVar
HNF1B c.544+1G>A
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg165His
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg165His
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Leu16fs
deletion
UNSPECDriverNot reportedClinVar
HNF1B p.Leu16fs
deletion
UNSPECDriverNot reportedClinVar
HNF1B p.His336Tyr
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.His336Tyr
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Pro159_Met160insTer
deletion
UNSPECDriverNot reportedClinVar
HNF1B p.Pro159_Met160insTer
deletion
UNSPECDriverNot reportedClinVar
HNF1B p.Arg295His
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg295His
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Ile403Phe
substitution
UNSPECVUSNot reportedClinVar
HNF1B p.Ile403Phe
substitution
UNSPECVUSNot reportedClinVar
HNF1B p.Arg181Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Arg181Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Gln182Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Gln182Ter
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Ile366fs
deletion
UNSPECDriverNot reportedClinVar
HNF1B p.Ile366fs
deletion
UNSPECDriverNot reportedClinVar
HNF1B p.Ser342Pro
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Ser342Pro
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Asn289Asp
substitution
UNSPECDriverNot reportedClinVar
HNF1B p.Asn289Asp
substitution
UNSPECDriverNot reportedClinVar