Gene dossier

SDHC

221 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
SDHC p.Met1Ile
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Met1Ile
substitution
UNSPECDriverNot reportedClinVar
SDHC c.405+1G>T
substitution
UNSPECDriverNot reportedClinVar
SDHC c.405+1G>T
substitution
UNSPECDriverNot reportedClinVar
SDHC ClinVar:7243
deletion
UNSPECDriverNot reportedClinVar
SDHC ClinVar:7243|UNSPEC
deletion
UNSPECDriverNot reportedClinVar
SDHC c.405+1G>A
substitution
UNSPECDriverNot reportedClinVar
SDHC c.405+1G>A
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Arg15Ter
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Arg15Ter
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Arg50Cys
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Arg50Cys
substitution
UNSPECDriverNot reportedClinVar
SDHC c.78-1G>A
substitution
UNSPECDriverNot reportedClinVar
SDHC c.78-1G>A
substitution
UNSPECDriverNot reportedClinVar
SDHC p.His127Arg
substitution
UNSPECDriverNot reportedClinVar
SDHC p.His127Arg
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Arg133Ter
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Arg133Ter
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Ala3fs
deletion
UNSPECDriverNot reportedClinVar
SDHC p.Ala3fs
deletion
UNSPECDriverNot reportedClinVar
SDHC p.Gly75Asp
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Gly75Asp
substitution
UNSPECDriverNot reportedClinVar
SDHC p.Tyr126fs
duplication
UNSPECDriverNot reportedClinVar
SDHC p.Tyr126fs
duplication
UNSPECDriverNot reportedClinVar
SDHC c.406-?_*2318+?del
deletion
UNSPECDriverNot reportedClinVar
SDHC c.179+1G>C
substitution
UNSPECDriverNot reportedClinVar
SDHC c.179+1G>C
substitution
UNSPECDriverNot reportedClinVar
SDHC ClinVar:417394
duplication
UNSPECDriverNot reportedClinVar
SDHC ClinVar:417394|UNSPEC
duplication
UNSPECDriverNot reportedClinVar
SDHC ClinVar:417389
deletion
UNSPECDriverNot reportedClinVar