Gene dossier

SDHB

658 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
SDHB p.Arg90Ter
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Arg90Ter
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Pro197Arg
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Pro197Arg
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Arg242His
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Arg242His
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Ser239fs
Microsatellite
UNSPECDriverNot reportedClinVar
SDHB p.Ser239fs
Microsatellite
UNSPECDriverNot reportedClinVar
SDHB p.Arg27Ter
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Arg27Ter
substitution
UNSPECDriverNot reportedClinVar
SDHB c.(-151_-1
deletion
UNSPECDriverNot reportedClinVar
SDHB p.Arg46Gly
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Arg46Gly
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Cys101Tyr
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Cys101Tyr
substitution
UNSPECDriverNot reportedClinVar
SDHB p.His132Pro
substitution
UNSPECDriverNot reportedClinVar
SDHB p.His132Pro
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Ser100Phe
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Ser100Phe
substitution
UNSPECDriverNot reportedClinVar
SDHB c.423+1G>C
substitution
UNSPECDriverNot reportedClinVar
SDHB c.423+1G>C
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Val140Phe
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Val140Phe
substitution
UNSPECDriverNot reportedClinVar
SDHB ClinVar:18455
deletion
UNSPECDriverNot reportedClinVar
SDHB ClinVar:18455|UNSPEC
deletion
UNSPECDriverNot reportedClinVar
SDHB ClinVar:18456
deletion
UNSPECDriverNot reportedClinVar
SDHB ClinVar:18456|UNSPEC
deletion
UNSPECDriverNot reportedClinVar
SDHB c.423+1G>A
substitution
UNSPECDriverNot reportedClinVar
SDHB c.423+1G>A
substitution
UNSPECDriverNot reportedClinVar
SDHB p.Arg11His
substitution
UNSPECVUSNot reportedClinVar