List of variants reported as benign for Nonpapillary renal cell carcinoma by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.51C>G (p.Leu17=)	rs1169289	0.42543
NM_000545.8(HNF1A):c.79A>C (p.Ile27Leu)	rs1169288	0.35489
NM_000545.8(HNF1A):c.1501+7G>A	rs2464195	0.30441
NM_000545.8(HNF1A):c.1460G>A (p.Ser487Asn)	rs2464196	0.26206
NM_000545.8(HNF1A):c.1375C>T (p.Leu459=)	rs2259820	0.26141
NM_000545.8(HNF1A):c.864G>C (p.Gly288=)	rs56348580	0.25042
NM_000545.8(HNF1A):c.1545G>A (p.Thr515=)	rs55834942	0.13864
NM_000545.8(HNF1A):c.293C>T (p.Ala98Val)	rs1800574	0.02065
NM_000545.8(HNF1A):c.326+20C>A	rs80051981	0.00772
NM_000458.4(HNF1B):c.345-19C>T	rs59527848	0.00765
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=)	rs140781855	0.00325
NM_000545.8(HNF1A):c.276C>T (p.Leu92=)	rs34056805	0.00269
NM_000545.8(HNF1A):c.252C>T (p.Pro84=)	rs78772552	0.00215
NM_000545.8(HNF1A):c.210C>T (p.Ser70=)	rs146686581	0.00061
NM_000458.4(HNF1B):c.73G>T (p.Val25Leu)	rs139107479	0.00015
NM_000545.8(HNF1A):c.-4A>G	rs561269721	0.00001

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.