List of variants in gene SLC22A5 reported by Mayo Clinic Laboratories, Mayo Clinic

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003060.4(SLC22A5):c.1142T>C (p.Met381Thr)	rs149730454	0.00056
NM_003060.4(SLC22A5):c.136C>T (p.Pro46Ser)	rs202088921	0.00052
NM_003060.4(SLC22A5):c.1451G>T (p.Gly484Val)	rs28383480	0.00039
NM_003060.4(SLC22A5):c.605T>C (p.Leu202Pro)	rs142447950	0.00035
NM_003060.4(SLC22A5):c.1643G>A (p.Arg548Lys)	rs150775371	0.00023
NM_003060.4(SLC22A5):c.695C>T (p.Thr232Met)	rs114269482	0.00018
NM_003060.4(SLC22A5):c.761G>A (p.Arg254Gln)	rs200699819	0.00007
NM_003060.4(SLC22A5):c.1193C>T (p.Pro398Leu)	rs144547521	0.00006
NM_003060.4(SLC22A5):c.811G>A (p.Val271Met)	rs143013773	0.00004
NM_003060.4(SLC22A5):c.420G>A (p.Trp140Ter)	rs2126775665

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.