SDHC

succinate dehydrogenase complex subunit C
OMIM: 602413, Gene2Phenotype

12 panels

Panel Reviews Mode of inheritance Details
12 panels

Green SDHC in Incidentalome


Version 0.301

review Unknown
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green SDHC in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 0.131

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Paragangliomas 3, MIM# 605373

Red SDHC in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.927

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review Unknown
    Sources
    • Expert Review Red
    Phenotypes
    • Mitochondrial disease MONDO:0044970

    Green SDHC in Additional findings_Adult


    Level 2: Screening
    Version 0.166

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Paragangliomas 3, MIM# 605373

    Red SDHC in CGC_86


    Version 0.2

    review Other
    Sources
    • CGC_86
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes
    • Paraganglioma and gastric stromal sarcoma

    Red SDHC in NCGC


    Version 0.2

    review Other
    Sources
    • NCGC
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes
    • Paraganglioma and gastric stromal sarcoma

    Red SDHC in TCGA_PANCAN_2018


    Version 0.2

    review Other
    Sources
    • TCGA_PANCAN_2018
    Phenotypes
    • Paraganglioma and gastric stromal sarcoma
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Green SDHC in Renal cancer


    Level 2: Cancer susceptibility
    Version 0.4

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • SA Pathology
    Phenotypes
    • Paragangiomas 3

    Amber SDHC in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • BabySeq Category B gene
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Green SDHC in Incidentalome_PREGEN_DRAFT


    Version 0.43

    review Unknown
    Sources
    • NSW Health Pathology
    • Expert Review Green

    Amber SDHC in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category B gene
    • Expert Review Amber
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Green SDHC in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Paragangliomas 3, MIM# 605373