List of variants in gene C1QC studied for C1Q deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_172369.5(C1QC):c.538G>A (p.Val180Met)	rs200292688	0.00006
NM_172369.5(C1QC):c.8T>C (p.Val3Ala)	rs367838299	0.00006
NM_172369.5(C1QC):c.100G>A (p.Gly34Arg)	rs200206736	0.00005
NM_172369.5(C1QC):c.490G>A (p.Gly164Ser)	rs752596663	0.00004
NM_172369.5(C1QC):c.706G>A (p.Val236Ile)	rs774542072	0.00002
NM_172369.5(C1QC):c.205C>T (p.Arg69Ter)	rs377549148	0.00001
NM_172369.5(C1QC):c.19_20delinsAA (p.Ser7Asn)	rs1557603993
NM_172369.5(C1QC):c.19delinsAA (p.Ser7fs)
NM_172369.5(C1QC):c.644AGG[1] (p.Glu216del)

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.