ClinVar Miner

List of variants in gene GALT reported as pathogenic for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_000155.3(GALT):c.855G>T (p.Lys285Asn) rs111033773
NM_001258332.1(GALT):c.125T>C (p.Val42Ala) rs111033701
NM_001258332.1(GALT):c.197G>A (p.Gly66Asp) rs111033718
NM_001258332.1(GALT):c.274C>T (p.Arg92Cys) rs111033739
NM_001258332.1(GALT):c.421C>A (p.Pro141Thr) rs111033759

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.