ClinVar Miner

Variants in gene CCNF

See also:
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
4 2 54 31 44 130

Condition and significance breakdown #

Total conditions: 7
Download table as spreadsheet
Condition pathogenic likely pathogenic uncertain significance likely benign benign total
not provided 0 1 12 16 43 70
not specified 0 0 36 7 0 43
CCNF-related disorder 0 0 0 9 1 10
Frontotemporal dementia and/or amyotrophic lateral sclerosis 5 4 0 5 0 0 9
Amyotrophic lateral sclerosis 0 0 1 0 0 1
Frontotemporal dementia 0 1 0 0 0 1
Polyneuropathy 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 17
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Ambry Genetics 0 0 35 7 0 42
GeneDx 0 0 5 0 35 40
Labcorp Genetics (formerly Invitae), Labcorp 0 0 3 10 8 21
Breakthrough Genomics, Breakthrough Genomics 0 0 0 1 18 19
PreventionGenetics, part of Exact Sciences 0 0 0 9 1 10
CeGaT Center for Human Genetics Tuebingen 0 1 2 6 1 10
OMIM 4 0 0 0 0 4
Mayo Clinic Laboratories, Mayo Clinic 0 0 2 0 0 2
Neuberg Centre For Genomic Medicine, NCGM 0 0 2 0 0 2
Baylor Genetics 0 0 1 0 0 1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 1 0 0 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 0 1 0 0 1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 1 0 0 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 1
Dept. of Medical Genetics, Telemark Hospital Trust, Telemark Hospital Trust 0 0 1 0 0 1
Guerreiro-Bras Laboratory, Van Andel Institute 0 1 0 0 0 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.