List of variants in gene FAM161A reported as benign by Natera, Inc.

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001201543.2(FAM161A):c.1212T>C (p.Cys404=)	rs4672457	0.98181
NM_001201543.2(FAM161A):c.706A>G (p.Ile236Val)	rs17513722	0.17102
NM_001201543.2(FAM161A):c.321A>G (p.Ile107Met)	rs11125895	0.16195
NM_001201543.2(FAM161A):c.1665G>A (p.Leu555=)	rs6545910	0.10308
NM_001201543.2(FAM161A):c.1655T>G (p.Met552Arg)	rs76112350	0.01067
NM_001201543.2(FAM161A):c.423-7C>T	rs144455077	0.00755
NM_001201543.2(FAM161A):c.906A>G (p.Gln302=)	rs76110744	0.00702
NM_001201543.2(FAM161A):c.1013G>A (p.Arg338Gln)	rs149314387	0.00644
NM_001201543.2(FAM161A):c.817G>A (p.Glu273Lys)	rs6733774	0.00570
NM_001201543.2(FAM161A):c.197C>T (p.Thr66Ile)	rs145199539	0.00372

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.