List of variants in gene HNF1A reported as likely benign for nonpapillary renal cell carcinoma

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.326+6_326+10dup	rs56158114	0.00415
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val)	rs115080759	0.00198
NM_000545.8(HNF1A):c.1446C>T (p.Ser482=)	rs147366495	0.00117
NM_000545.8(HNF1A):c.1323G>A (p.Thr441=)	rs138996307	0.00081
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp)	rs137853247	0.00076
NM_000545.8(HNF1A):c.1386C>T (p.Val462=)	rs143015301	0.00021
NM_000545.8(HNF1A):c.1108-4G>A	rs372892932	0.00020
NM_000545.8(HNF1A):c.1377G>A (p.Leu459=)	rs118028009	0.00020
NM_000545.8(HNF1A):c.1071G>A (p.Glu357=)	rs376279459	0.00006
NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser)	rs766790596	0.00004
NM_000545.8(HNF1A):c.150C>T (p.Cys50=)	rs193922583	0.00004
NM_000545.8(HNF1A):c.713+13G>A	rs755961371	0.00004
NM_000545.8(HNF1A):c.153C>T (p.Gly51=)	rs761779651	0.00001
NM_000545.8(HNF1A):c.685C>A (p.Arg229=)	rs769086289	0.00001
NM_000545.8(HNF1A):c.-167TGGGGGT[3]	rs538476099
NM_000545.8(HNF1A):c.1719_1720inv (p.Ser574Gly)
NM_000545.8(HNF1A):c.498C>T (p.Tyr166=)	rs1876675633

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.