List of variants in gene RPGRIP1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.930+3A>G	rs150107283	0.00419
NM_020366.4(RPGRIP1):c.1767G>T (p.Gln589His)	rs34067949	0.00344
NM_020366.4(RPGRIP1):c.2284C>T (p.Leu762=)	rs145896974	0.00240
NM_020366.4(RPGRIP1):c.1753C>T (p.Pro585Ser)	rs147586703	0.00155
NM_020366.4(RPGRIP1):c.95T>A (p.Met32Lys)	rs200510462	0.00140
NM_020366.4(RPGRIP1):c.3171C>T (p.His1057=)	rs201838837	0.00053
NM_020366.4(RPGRIP1):c.1920C>T (p.Ala640=)	rs368434311	0.00029
NM_020366.4(RPGRIP1):c.2435G>A (p.Arg812Gln)	rs190490019	0.00024
NM_020366.4(RPGRIP1):c.2592T>C (p.Tyr864=)	rs201639860	0.00004
NM_020366.4(RPGRIP1):c.1197C>T (p.Asn399=)	rs372186092	0.00003
NM_020366.4(RPGRIP1):c.1692A>G (p.Leu564=)
NM_020366.4(RPGRIP1):c.2040C>T (p.Ser680=)

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.