List of variants in gene NEXMIF reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.133G>A (p.Ala45Thr)	rs199960807	0.00030
NM_001008537.3(NEXMIF):c.206C>T (p.Ser69Phe)	rs201351157	0.00014
NM_001008537.3(NEXMIF):c.3402C>A (p.His1134Gln)	rs138632224	0.00011
NM_001008537.3(NEXMIF):c.3386T>G (p.Phe1129Cys)	rs202207238	0.00006
NM_001008537.3(NEXMIF):c.381G>A (p.Glu127=)	rs148717498	0.00005
NM_001008537.3(NEXMIF):c.2130G>A (p.Lys710=)	rs749479992	0.00004
NM_001008537.3(NEXMIF):c.3319G>A (p.Asp1107Asn)	rs751468762	0.00002
NM_001008537.3(NEXMIF):c.4243A>G (p.Met1415Val)	rs797045648	0.00001
NM_001008537.3(NEXMIF):c.1998AGA[1] (p.Glu667del)	rs764439412
NM_001008537.3(NEXMIF):c.2406T>A (p.Asn802Lys)	rs1307046706
NM_001008537.3(NEXMIF):c.2560C>A (p.Pro854Thr)	rs797045645
NM_001008537.3(NEXMIF):c.3972C>T (p.Ala1324=)	rs797045647

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.