ClinVar Miner

List of variants in gene SLC33A1 reported as uncertain significance for Spastic paraplegia, autosomal dominant

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_004733.3(SLC33A1):c.*1200T>C rs886058102
NM_004733.3(SLC33A1):c.*1230A>G rs886058101
NM_004733.3(SLC33A1):c.*149C>T rs886058107
NM_004733.3(SLC33A1):c.*1529C>T rs886058100
NM_004733.3(SLC33A1):c.*509G>T rs886058106
NM_004733.3(SLC33A1):c.*582_*583delAA rs762573505
NM_004733.3(SLC33A1):c.*595A>C rs886058105
NM_004733.3(SLC33A1):c.*746T>G rs774751936
NM_004733.3(SLC33A1):c.*755C>T rs189496085
NM_004733.3(SLC33A1):c.*869G>A rs886058104
NM_004733.3(SLC33A1):c.*893delT rs886058103
NM_004733.3(SLC33A1):c.-27C>T rs777838988
NM_004733.3(SLC33A1):c.-281C>T rs560777515
NM_004733.3(SLC33A1):c.1068G>A (p.Gln356=) rs886058108
NM_004733.3(SLC33A1):c.1149-4A>G rs773106675
NM_004733.3(SLC33A1):c.1267-4G>A rs779467886
NM_004733.3(SLC33A1):c.131G>T (p.Gly44Val) rs780400607
NM_004733.3(SLC33A1):c.613T>C (p.Leu205=) rs886058110
NM_004733.3(SLC33A1):c.904T>C (p.Phe302Leu) rs886058109

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.