ClinVar Miner

Variants studied for Lung cancer

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign confers sensitivity not provided total
3 16 11 57 108 4 1 199

Gene and significance breakdown #

Total genes and gene combinations: 17
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign confers sensitivity not provided total
EGFR 2 2 9 56 108 0 1 177
ALK 0 4 0 0 0 0 0 4
KRAS 0 3 0 0 0 0 0 3
KMT2D 0 2 0 0 0 0 0 2
ATM 0 0 1 0 0 0 0 1
BARD1 0 0 0 1 0 0 0 1
BMP2 0 0 0 0 0 1 0 1
CASP8 0 1 0 0 0 0 0 1
ERBB2 0 0 1 0 0 0 0 1
FASLG 0 1 0 0 0 0 0 1
MLH1 0 1 0 0 0 0 0 1
NFE2L2 0 1 0 0 0 0 0 1
PALB2 1 0 0 0 0 0 0 1
SLC19A1 0 1 0 0 0 0 0 1
SMAD3 0 0 0 0 0 1 0 1
SMAD4 0 0 0 0 0 1 0 1
SMAD9 0 0 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign confers sensitivity not provided total
Myriad Genetics, Inc. 0 1 0 47 102 0 0 150
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 8 11 0 0 19
Molekularpathologisches Zentrum, Universitaetsklinikum Heidelberg 1 8 0 0 0 0 0 9
Baylor Genetics 0 0 6 0 0 0 0 6
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 2 3 0 0 0 0 5
Kong Lab, Department of Radiation Oncology, Case Western Reserve University School of Medicine 0 0 0 0 0 4 0 4
Key Laboratory of Carcinogenesis and Cancer Invasion, Central South University 0 3 0 0 0 0 0 3
OMIM 1 0 0 0 0 0 0 1
Mendelics 0 0 0 1 0 0 0 1
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 0 1 0 0 0 0 0 1
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 0 1 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 0 1 0 0 0 0 1
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 0 1 1
Neuberg Centre For Genomic Medicine, NCGM 1 0 0 0 0 0 0 1
Department of Laboratory Medicine, Maanshan College 1 0 0 0 0 0 0 1
BioPath Innovations S.A. 0 0 1 0 0 0 0 1
Scientific Research Center, Shenzhen Evergreen Medical Institute 0 1 0 0 0 0 0 1

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