ClinVar Miner

Variants studied for Prostate cancer, hereditary, 1

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 total
2 0 1294 0 0 1295

Gene and significance breakdown #

Total genes and gene combinations: 8
Download table as spreadsheet
Gene or gene combination pathogenic uncertain significance total
HOXB13 0 762 762
PTEN 0 141 141
BRAF 0 126 126
TP53 0 110 110
RNASEL 2 75 76
KRAS 0 72 72
HRAS, LRRC56 0 6 6
NRAS 0 2 2

Submitter and significance breakdown #

Total submitters: 8
Download table as spreadsheet
Submitter pathogenic uncertain significance total
Laboratory of Virology, Microbiology, Quality and Medical Biotechnologies, Faculty of Sciences and Techniques - Mohammedia, Hassan II University of Casablanca 0 762 762
Laboratory of Virology, Oncology, Biosciences and Environment, Faculty of Sciences and Techniques, Mohammedia- University Hassan II of Casablanca 0 525 525
OMIM 2 0 2
Revvity Omics, Revvity 0 2 2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 2 2
Institute of Human Genetics, University of Leipzig Medical Center 0 1 1
Neuberg Centre For Genomic Medicine, NCGM 0 1 1
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 1 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.