ClinVar Miner

List of variants in gene COMP reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000095.3(COMP):c.1915-45C>T rs12327738 0.29386
NM_000095.3(COMP):c.2228-40T>C rs28494505 0.21598
NM_000095.3(COMP):c.165+41G>C rs35359254 0.15497
NM_000095.3(COMP):c.2267A>G (p.Gln756Arg) rs61752496 0.06295
NM_000095.3(COMP):c.*1G>C rs77185131 0.06291
NM_000095.3(COMP):c.1755G>A (p.Thr585=) rs34467947 0.04927
NM_000095.3(COMP):c.1156A>G (p.Asn386Asp) rs61739916 0.03133
NM_000095.3(COMP):c.511G>A (p.Ala171Thr) rs115338183 0.01840
NM_000095.3(COMP):c.762+12C>A rs199733531 0.00463
NM_000095.3(COMP):c.1488C>A (p.Asp496Glu) rs143714206 0.00081
NM_000095.3(COMP):c.218-7C>G rs554031979 0.00051
NM_000095.3(COMP):c.924C>T (p.Ile308=) rs199596155 0.00007
NM_000095.3(COMP):c.1255-5C>T rs201124517 0.00006
NM_000095.3(COMP):c.1590C>A (p.Asp530Glu) rs759687021 0.00003
NM_000095.3(COMP):c.1563G>A (p.Pro521=) rs756075225 0.00001
NM_000095.3(COMP):c.1317C>A (p.Asp439Glu)
NM_000095.3(COMP):c.1384G>T (p.Asp462Tyr)
NM_000095.3(COMP):c.1411G>C (p.Asp471His)
NM_000095.3(COMP):c.1587C>T (p.Thr529=)
NM_000095.3(COMP):c.1755G>T (p.Thr585=) rs34467947
NM_000095.3(COMP):c.218-14C>T rs150008764
NM_000095.3(COMP):c.218-6C>A rs534407430
NM_000095.3(COMP):c.686G>A (p.Cys229Tyr)
NM_000095.3(COMP):c.964C>T (p.Pro322Ser)

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.