ClinVar Miner

List of variants in gene VPS13B reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 8q22.2(chr8:100133404-100133674)x1
NM_015243.2(VPS13B):c.1700G>A (p.Gly567Glu) rs141046414
NM_017890.4(VPS13B):c.3346_3347CT[1] (p.Cys1117fs) rs180177327
NM_017890.4(VPS13B):c.3397C>T (p.Pro1133Ser) rs781781537
NM_017890.4(VPS13B):c.6732+1G>A rs180177366
NM_017890.4(VPS13B):c.9260dupT (p.Leu3087Phefs) rs180177329

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.