List of variants in gene NDP reported as benign 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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000266.4(NDP):c.-208+206C>G	rs1159223	0.33835
NC_000023.11:g.43973680T>A	rs12843168	0.24966
NM_000266.4(NDP):c.174+42A>G	rs112278531	0.03232
NM_000266.4(NDP):c.-111G>T	rs45501198	0.01698
NM_000266.4(NDP):c.*10C>G	rs140653237	0.00580
NM_000266.4(NDP):c.69C>G (p.Asp23Glu)	rs5952410	0.00538
NM_000266.4(NDP):c.11A>T (p.His4Leu)	rs149708528	0.00012
NM_000266.4(NDP):c.165T>C (p.Cys55=)	rs201271933	0.00009
NM_000266.4(NDP):c.101C>T (p.Ser34Leu)	rs144031424	0.00003
NM_000266.4(NDP):c.269G>A (p.Arg90His)	rs104894867	0.00003
NM_000266.4(NDP):c.387G>A (p.Glu129=)	rs778584609	0.00001
NC_000023.11:g.43973757_43973764dup	rs17147234
NM_000266.3(NDP):c.-421_-408CTCTCTCTCTCTCC[1]	rs770996360
NM_000266.4(NDP):c.174+19_174+20del	rs375616103
NM_000266.4(NDP):c.175-143dup	rs112297052
NM_000266.4(NDP):c.175-252del	rs200013146

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.