List of variants in gene MT-ND5 reported as likely benign for Leigh syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 48

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND5):m.12340A>G	rs28490236
NC_012920.1(MT-ND5):m.12341C>T	rs1603223671
NC_012920.1(MT-ND5):m.12352A>G	rs1603223680
NC_012920.1(MT-ND5):m.12367A>G	rs1603223696
NC_012920.1(MT-ND5):m.12401C>T	rs1603223721
NC_012920.1(MT-ND5):m.12424A>G	rs1603223732
NC_012920.1(MT-ND5):m.12436C>T	rs1603223738
NC_012920.1(MT-ND5):m.12437A>G	rs1603223739
NC_012920.1(MT-ND5):m.12451A>G	rs1603223750
NC_012920.1(MT-ND5):m.12481T>A	rs1603223762
NC_012920.1(MT-ND5):m.12512A>T	rs1603223776
NC_012920.1(MT-ND5):m.12622G>A	rs1603223840
NC_012920.1(MT-ND5):m.12661A>T	rs1603223854
NC_012920.1(MT-ND5):m.12674A>G	rs1603223860
NC_012920.1(MT-ND5):m.12730G>A	rs1603223879
NC_012920.1(MT-ND5):m.12890C>T	rs1603223958
NC_012920.1(MT-ND5):m.12906C>A	rs28690070
NC_012920.1(MT-ND5):m.13153A>G	rs878957731
NC_012920.1(MT-ND5):m.13225G>A	rs1603224098
NC_012920.1(MT-ND5):m.13285A>G	rs1603224130
NC_012920.1(MT-ND5):m.13466G>A	rs3902404
NC_012920.1(MT-ND5):m.13543T>C	rs1603224227
NC_012920.1(MT-ND5):m.13576A>G	rs1603224243
NC_012920.1(MT-ND5):m.13579G>A	rs1603224246
NC_012920.1(MT-ND5):m.13606A>G	rs1603224258
NC_012920.1(MT-ND5):m.13615A>G	rs1603224265
NC_012920.1(MT-ND5):m.13649C>T	rs1603224283
NC_012920.1(MT-ND5):m.13661A>G	rs1603224293
NC_012920.1(MT-ND5):m.13676A>G	rs1603224300
NC_012920.1(MT-ND5):m.13681A>T	rs386829187
NC_012920.1(MT-ND5):m.13762T>A	rs879154715
NC_012920.1(MT-ND5):m.13763C>T	rs1603224344
NC_012920.1(MT-ND5):m.13768T>A	rs1556424325
NC_012920.1(MT-ND5):m.13770C>A	rs1603224349
NC_012920.1(MT-ND5):m.13790A>G	rs1556424326
NC_012920.1(MT-ND5):m.13801A>G	rs1603224358
NC_012920.1(MT-ND5):m.13816A>G	rs1603224365
NC_012920.1(MT-ND5):m.13879T>A	rs879087566
NC_012920.1(MT-ND5):m.13888T>C	rs1603224403
NC_012920.1(MT-ND5):m.13907A>G	rs1603224408
NC_012920.1(MT-ND5):m.13919T>A	rs1603224418
NC_012920.1(MT-ND5):m.14029A>G	rs1603224478
NC_012920.1(MT-ND5):m.14035T>G	rs1556424374
NC_012920.1(MT-ND5):m.14040G>C	rs57180882
NC_012920.1(MT-ND5):m.14047A>G	rs1603224486
NC_012920.1(MT-ND5):m.14060T>C	rs1603224503
NC_012920.1(MT-ND5):m.14062A>G	rs1603224506
NC_012920.1(MT-ND5):m.14142C>A	rs1603224552

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.