List of variants in gene NDRG1 reported 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
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006096.4(NDRG1):c.331A>C (p.Met111Leu)	rs2233328	0.00201
NM_006096.4(NDRG1):c.31G>A (p.Ala11Thr)	rs145871479	0.00140
NM_006096.4(NDRG1):c.122A>G (p.His41Arg)	rs2233318	0.00054
NM_006096.4(NDRG1):c.664G>A (p.Gly222Ser)	rs199995009	0.00015
NM_006096.4(NDRG1):c.1088G>A (p.Arg363His)	rs181121989	0.00014
NM_006096.4(NDRG1):c.1101C>T (p.Ser367=)	rs201959970	0.00007
NM_006096.4(NDRG1):c.1022G>A (p.Arg341His)	rs1392179290	0.00001
NM_006096.4(NDRG1):c.1085G>A (p.Ser362Asn)	rs749124058	0.00001
NM_006096.4(NDRG1):c.442C>T (p.Arg148Ter)	rs119483085	0.00001
NM_006096.4(NDRG1):c.1053_1082del (p.340TRSRSHTSEG[2])	rs751274009
NM_006096.4(NDRG1):c.1062_1091del (p.340_349TRSRSHTSEG[2])	rs763499117
NM_006096.4(NDRG1):c.1064A>C (p.His355Pro)
NM_006096.4(NDRG1):c.389+7G>C
NM_006096.4(NDRG1):c.397A>G (p.Ser133Gly)
NM_006096.4(NDRG1):c.432C>T (p.Tyr144=)	rs535684670
NM_006096.4(NDRG1):c.462T>G (p.Pro154=)

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.