List of variants in gene combination C17orf107, CHRNE reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000080.4(CHRNE):c.235-25C>T	rs140756451	0.00236
NM_000080.4(CHRNE):c.344+18C>T	rs201821934	0.00145
NM_000080.4(CHRNE):c.555C>T (p.Asp185=)	rs137952354	0.00096
NM_000080.4(CHRNE):c.901G>A (p.Val301Met)	rs140023380	0.00046
NM_000080.4(CHRNE):c.23T>C (p.Val8Ala)	rs199807050	0.00026
NM_000080.4(CHRNE):c.797C>T (p.Ala266Val)	rs201463598	0.00016
NM_000080.4(CHRNE):c.465C>T (p.Phe155=)	rs139625105	0.00009
NM_000080.4(CHRNE):c.6A>G (p.Ala2=)	rs202198207	0.00008
NM_000080.4(CHRNE):c.174G>A (p.Thr58=)	rs373275223	0.00006
NM_000080.4(CHRNE):c.462C>T (p.Tyr154=)	rs781427923	0.00005
NM_000080.4(CHRNE):c.237T>C (p.Asp79=)	rs777458923	0.00002
NM_000080.4(CHRNE):c.852C>T (p.Thr284=)	rs770586668	0.00002
NM_000080.4(CHRNE):c.420T>C (p.Pro140=)	rs886038226	0.00001
NM_000080.4(CHRNE):c.500+39G>A	rs201470386
NM_001145536.2(C17orf107):c.*377GGAG[1]	rs762704832

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.