ERCC3 Chromosome 2

ERCC excision repair 3, TFIIH core complex helicase subunit
78 variants 78 Health Risk

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What This Gene Does
This gene encodes an ATP-dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Gene Info
Gene Group
"Xeroderma pigmentosum complementation groups|ERCC excision repair associated|General transcription factor IIH complex subunits|DexD/H helicases"
Locus Type
gene with protein product
Location
2q14.3
Ensembl
ENSG00000163161
Associated Conditions (11)
Xeroderma pigmentosum group B
Xeroderma pigmentosum
Trichothiodystrophy 2
photosensitive
Inborn genetic diseases
Ovarian cancer
ERCC3-related disorder
Thyroid cancer
nonmedullary
1
Hereditary cancer-predisposing syndrome
Key Variants
RS114508982
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
Health Risk
RS114710997
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
Health Risk
RS1194673433
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
Health Risk
RS1258857605
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
Health Risk
RS1419254389
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
Health Risk
RS142333442
Conflicting classifications of pathogenicity
Health Risk
RS145201970
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Trichothiodystrophy 2, photosensitive
Health Risk
RS145830873
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
Health Risk
RS151216904
Conflicting classifications of pathogenicity
Xeroderma pigmentosum group B, Xeroderma pigmentosum, Trichothiodystrophy 2
Health Risk
RS1684835050
Conflicting classifications of pathogenicity
Ovarian cancer, Inborn genetic diseases, Ovarian cancer
Health Risk
RS200098409
Conflicting classifications of pathogenicity
Ovarian cancer, Ovarian cancer
Health Risk
RS200361738
Conflicting classifications of pathogenicity
Xeroderma pigmentosum, Xeroderma pigmentosum
Health Risk
All Variants (78)
RSID Category Clinical Significance Conditions
RS114508982 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS114710997 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS1194673433 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS1258857605 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS1419254389 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS142333442 Health Risk Conflicting classifications of pathogenicity
RS145201970 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Trichothiodystrophy 2, photosensitive
RS145830873 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS151216904 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Trichothiodystrophy 2
RS1684835050 Health Risk Conflicting classifications of pathogenicity Ovarian cancer, Inborn genetic diseases, Ovarian cancer
RS200098409 Health Risk Conflicting classifications of pathogenicity Ovarian cancer, Ovarian cancer
RS200361738 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, Xeroderma pigmentosum
RS200733704 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B, Xeroderma pigmentosum
RS200833462 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS201054106 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS369227601 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, Xeroderma pigmentosum
RS371396764 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS375556869 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS376593226 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, ERCC3-related disorder
RS377391723 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS529637184 Health Risk Conflicting classifications of pathogenicity Trichothiodystrophy 2, photosensitive, ERCC3-related disorder
RS531561069 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS568193912 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, ERCC3-related disorder, Inborn genetic diseases
RS746754189 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS752026166 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS764062606 Health Risk Conflicting classifications of pathogenicity Ovarian cancer, Ovarian cancer
RS765724086 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum, Xeroderma pigmentosum
RS769083884 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS770925947 Health Risk Conflicting classifications of pathogenicity Trichothiodystrophy 2, photosensitive, Xeroderma pigmentosum group B
RS774063464 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS781533251 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS886054844 Health Risk Conflicting classifications of pathogenicity Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS1237725504 Health Risk Likely pathogenic Ovarian cancer, Ovarian cancer
RS1404157087 Health Risk Likely pathogenic Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS1420747225 Health Risk Likely pathogenic Xeroderma pigmentosum, Xeroderma pigmentosum
RS56116802 Health Risk Likely pathogenic Xeroderma pigmentosum, Xeroderma pigmentosum group B, Trichothiodystrophy 2
RS755760603 Health Risk Likely pathogenic Xeroderma pigmentosum group B, Trichothiodystrophy 2, photosensitive
RS1200552239 Health Risk Pathogenic
RS121913045 Health Risk Pathogenic Xeroderma pigmentosum group B, Trichothiodystrophy 2, photosensitive
RS121913046 Health Risk Pathogenic Trichothiodystrophy 2, photosensitive, Trichothiodystrophy 2
RS121913047 Health Risk Pathogenic Xeroderma pigmentosum group B, Inborn genetic diseases, Trichothiodystrophy 2
RS121913048 Health Risk Pathogenic Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS138385061 Health Risk Pathogenic Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS1391179566 Health Risk Pathogenic
RS1404293670 Health Risk Pathogenic Xeroderma pigmentosum group B, Xeroderma pigmentosum group B
RS1558964705 Health Risk Pathogenic Xeroderma pigmentosum group B, Xeroderma pigmentosum, Xeroderma pigmentosum group B
RS1685190008 Health Risk Pathogenic
RS1685202380 Health Risk Pathogenic
RS1685354796 Health Risk Pathogenic
RS2104762167 Health Risk Pathogenic
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