List of variants in gene RPGRIP1L reported as likely pathogenic for not provided

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_015272.5(RPGRIP1L):c.3446T>A (p.Ile1149Asn)	rs766943204	0.00006
NM_015272.5(RPGRIP1L):c.583A>T (p.Lys195Ter)	rs1277577195	0.00004
NM_015272.5(RPGRIP1L):c.2050C>T (p.Gln684Ter)	rs121918204	0.00002
NM_015272.5(RPGRIP1L):c.1372G>T (p.Glu458Ter)	rs776941281	0.00001
NM_015272.5(RPGRIP1L):c.71dup (p.Met24fs)	rs990678342	0.00001
NM_015272.5(RPGRIP1L):c.1104-2A>G
NM_015272.5(RPGRIP1L):c.1421del (p.Asn474fs)	rs760952407
NM_015272.5(RPGRIP1L):c.1694_1695del (p.Leu565fs)
NM_015272.5(RPGRIP1L):c.2027del (p.Asn676fs)	rs2151125463
NM_015272.5(RPGRIP1L):c.3187G>T (p.Glu1063Ter)	rs1057520162
NM_015272.5(RPGRIP1L):c.403del (p.Ser135fs)	rs1598411105
NM_015272.5(RPGRIP1L):c.632T>A (p.Leu211Ter)
NM_015272.5(RPGRIP1L):c.931del (p.Asp311fs)
NM_015272.5(RPGRIP1L):c.94dup (p.Thr32fs)
NM_015272.5(RPGRIP1L):c.972del (p.Cys325fs)	rs757594906

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.