ClinVar Miner

List of variants in gene CR2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001006658.3(CR2):c.2611G>T (p.Val871Leu) rs144572703 0.00319
NM_001006658.3(CR2):c.2352T>C (p.Ile784=) rs142319454 0.00170
NM_001006658.3(CR2):c.1458T>C (p.Phe486=) rs147378770 0.00115
NM_001006658.3(CR2):c.2844G>A (p.Glu948=) rs61754518 0.00098
NM_001006658.3(CR2):c.2747C>T (p.Thr916Ile) rs61754517 0.00033
NM_001006658.3(CR2):c.276T>G (p.Pro92=) rs371546344 0.00006
NM_001006658.3(CR2):c.21C>T (p.Leu7=) rs779365020 0.00005
NM_001006658.3(CR2):c.621C>T (p.Pro207=) rs573346582 0.00003
NM_001006658.3(CR2):c.3261A>G (p.Pro1087=) rs374978382 0.00001
NM_001006658.3(CR2):c.2225C>T (p.Thr742Met)
NM_001006658.3(CR2):c.524C>T (p.Pro175Leu) rs75282758
NM_001006658.3(CR2):c.624C>A (p.Pro208=) rs61759494

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.