List of variants in gene SLC17A8 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_139319.3(SLC17A8):c.54G>A (p.Lys18=)	rs11568528	0.00987
NM_139319.3(SLC17A8):c.355-4C>A	rs11568531	0.00670
NM_139319.3(SLC17A8):c.858T>C (p.Tyr286=)	rs148882860	0.00261
NM_139319.3(SLC17A8):c.658G>A (p.Ala220Thr)	rs11568530	0.00024
NM_139319.3(SLC17A8):c.232A>G (p.Ile78Val)	rs141811441	0.00007
NM_139319.3(SLC17A8):c.1330C>T (p.Arg444Cys)	rs374159026	0.00004

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.