ClinVar Miner

List of variants in gene SBF2 reported by Inherited Neuropathy Consortium

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_030962.3(SBF2):c.1066C>T (p.Arg356Ter) rs1032796987
NM_030962.3(SBF2):c.1459C>T (p.Arg487Ter) rs120074139
NM_030962.3(SBF2):c.1537C>T (p.Gln513Ter) rs1480710758
NM_030962.3(SBF2):c.4299G>C (p.Arg1433Ser) rs1590131053
NM_030962.3(SBF2):c.4443+1G>C rs1564872328
NM_030962.3(SBF2):c.4782T>G (p.Tyr1594Ter) rs1384571991
NM_030962.3(SBF2):c.862-2A>G rs1590716243

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.