ClinVar Miner

List of variants in gene STS studied for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_000351.6(STS):c.1022C>T (p.Ser341Leu) rs137853167
NM_000351.6(STS):c.1114T>A (p.Trp372Arg) rs137853165
NM_000351.6(STS):c.1115G>C (p.Trp372Ser) rs137853168
NM_000351.6(STS):c.1126A>G (p.Ile376Val) rs748174656
NM_000351.6(STS):c.1256+1G>T rs1601748137
NM_000351.6(STS):c.1331A>G (p.His444Arg) rs137853169
NM_000351.6(STS):c.1337G>A (p.Cys446Tyr) rs137853166
NM_000351.6(STS):c.287G>A (p.Trp96Ter) rs1463414987

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.