List of variants in gene TMEM231 reported as 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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001077418.3(TMEM231):c.582+17T>A	rs2738801	0.27293
NM_001077418.3(TMEM231):c.*8A>G	rs2242407	0.25393
NM_001077418.3(TMEM231):c.-6G>C	rs3743602	0.21908
NM_001077418.3(TMEM231):c.16C>G (p.Leu6Val)	rs3743601	0.10494
NM_001077418.3(TMEM231):c.813G>A (p.Val271=)	rs2242406	0.08287
NM_001077418.3(TMEM231):c.582+8C>G	rs144252983	0.02257
NM_001077418.3(TMEM231):c.582+3A>G	rs114290622	0.01823
NM_001077418.3(TMEM231):c.177G>C (p.Pro59=)	rs78196225	0.01307
NM_001077418.3(TMEM231):c.891G>A (p.Val297=)	rs149888762	0.00375

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.