List of variants in gene SPTLC1 studied for Amyotrophic lateral sclerosis 27, juvenile

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_006415.4(SPTLC1):c.112CTT[1] (p.Leu39del)	rs1197928094
NM_006415.4(SPTLC1):c.113T>G (p.Leu38Arg)
NM_006415.4(SPTLC1):c.118_123del (p.Phe40_Ser41del)	rs2118840030
NM_006415.4(SPTLC1):c.58G>T (p.Ala20Ser)	rs879254294
NM_006415.4(SPTLC1):c.68A>T (p.Tyr23Phe)	rs1554716504
NM_006415.4(SPTLC1):c.992C>A (p.Ser331Tyr)	rs267607087

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.