ClinVar Miner

List of variants in gene MT-ATP8 studied for Leigh syndrome

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ATP8):m.8369C>T rs1603221429
NC_012920.1(MT-ATP8):m.8373A>G rs1603221431
NC_012920.1(MT-ATP8):m.8373A>T rs1603221431
NC_012920.1(MT-ATP8):m.8379A>G rs1603221434
NC_012920.1(MT-ATP8):m.8381A>G rs1603221438
NC_012920.1(MT-ATP8):m.8381A>T rs1603221438
NC_012920.1(MT-ATP8):m.8382C>T rs1556423437
NC_012920.1(MT-ATP8):m.8387G>A rs1556423439
NC_012920.1(MT-ATP8):m.8388T>C rs879199176
NC_012920.1(MT-ATP8):m.8393C>T rs1556423442
NC_012920.1(MT-ATP8):m.8394C>T rs1603221450
NC_012920.1(MT-ATP8):m.8396A>G rs1603221454
NC_012920.1(MT-ATP8):m.8397C>G rs1603221456
NC_012920.1(MT-ATP8):m.8400T>C rs1603221459
NC_012920.1(MT-ATP8):m.8403T>C rs1603221460
NC_012920.1(MT-ATP8):m.8406C>T rs1556423448
NC_012920.1(MT-ATP8):m.8411A>C rs878942289
NC_012920.1(MT-ATP8):m.8411A>G rs878942289
NC_012920.1(MT-ATP8):m.8412T>C rs1556423451
NC_012920.1(MT-ATP8):m.8414C>T rs28358884
NC_012920.1(MT-ATP8):m.8415T>C rs1603221470
NC_012920.1(MT-ATP8):m.8417C>T rs199616772
NC_012920.1(MT-ATP8):m.8426T>C rs1556423461
NC_012920.1(MT-ATP8):m.8427T>C
NC_012920.1(MT-ATP8):m.8429C>T rs1603221477
NC_012920.1(MT-ATP8):m.8430T>C rs1603221478
NC_012920.1(MT-ATP8):m.8433T>C rs1603221480
NC_012920.1(MT-ATP8):m.8435A>G rs1603221481
NC_012920.1(MT-ATP8):m.8435A>T rs1603221481
NC_012920.1(MT-ATP8):m.8448T>C rs879056797
NC_012920.1(MT-ATP8):m.8453A>G rs1603221486
NC_012920.1(MT-ATP8):m.8454A>G rs1603221488
NC_012920.1(MT-ATP8):m.8460A>G rs1116906
NC_012920.1(MT-ATP8):m.8461C>A rs1603221493
NC_012920.1(MT-ATP8):m.8462T>C rs1603221496
NC_012920.1(MT-ATP8):m.8463A>G rs1603221498
NC_012920.1(MT-ATP8):m.8466A>G rs1603221500
NC_012920.1(MT-ATP8):m.8469T>C rs1603221503
NC_012920.1(MT-ATP8):m.8471C>T rs1603221506
NC_012920.1(MT-ATP8):m.8472C>T rs879209186
NC_012920.1(MT-ATP8):m.8474C>T rs1603221515
NC_012920.1(MT-ATP8):m.8477T>C rs1603221517
NC_012920.1(MT-ATP8):m.8478C>T rs201902227
NC_012920.1(MT-ATP8):m.8480C>T rs1603221520
NC_012920.1(MT-ATP8):m.8481C>T rs1603221521
NC_012920.1(MT-ATP8):m.8489A>G rs1603221529
NC_012920.1(MT-ATP8):m.8490T>C rs1603221530
NC_012920.1(MT-ATP8):m.8496T>C rs1603221534
NC_012920.1(MT-ATP8):m.8502A>G rs879247004
NC_012920.1(MT-ATP8):m.8502A>T rs879247004
NC_012920.1(MT-ATP8):m.8504T>C rs1603221542
NC_012920.1(MT-ATP8):m.8507A>G rs1603221546
NC_012920.1(MT-ATP8):m.8508A>G rs1603221548
NC_012920.1(MT-ATP8):m.8514C>T rs1603221554
NC_012920.1(MT-ATP8):m.8516T>C rs878928585
NC_012920.1(MT-ATP8):m.8519G>A rs878853091
NC_012920.1(MT-ATP8):m.8520A>G rs1603221561
NC_012920.1(MT-ATP8):m.8522C>T rs1603221562

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.