ClinVar Miner

List of variants reported as pathogenic for hereditary spastic paraplegia 11 by Mendelics

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025137.4(SPG11):c.2013_2026dup (p.Lys676fs) rs1595898078
NM_025137.4(SPG11):c.2048G>A (p.Trp683Ter) rs1595898030
NM_025137.4(SPG11):c.2444+1G>C rs312262743
NM_025137.4(SPG11):c.334G>T (p.Glu112Ter) rs1595940058
NM_025137.4(SPG11):c.4434+1G>A rs1567148391
NM_025137.4(SPG11):c.529_533del (p.Ile177fs) rs312262716
NM_025137.4(SPG11):c.592C>T (p.Gln198Ter) rs863225440
NM_025137.4(SPG11):c.6632dup (p.Pro2212fs) rs863225439
NM_025137.4(SPG11):c.6832_6833del (p.Ser2278fs) rs312262784

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.