List of variants in gene COL9A1 studied for perceptual disorders

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001851.6(COL9A1):c.902C>T (p.Pro301Leu)	rs192047082	0.00083
NM_001851.6(COL9A1):c.2159G>A (p.Arg720Gln)	rs192467838	0.00041
NM_001851.6(COL9A1):c.1553A>T (p.Asp518Val)	rs142539130	0.00019
NM_001851.6(COL9A1):c.158A>G (p.Asp53Gly)	rs564421091	0.00016
NM_001851.6(COL9A1):c.2456C>T (p.Pro819Leu)	rs144581626	0.00001
NM_001851.6(COL9A1):c.115G>A (p.Gly39Ser)
NM_001851.6(COL9A1):c.23C>T (p.Pro8Leu)
NM_001851.6(COL9A1):c.2617C>T (p.Arg873Ter)
NM_001851.6(COL9A1):c.2644del (p.Val882fs)	rs2127544065
NM_001851.6(COL9A1):c.82C>T (p.Arg28Cys)	rs745566207

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.