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: 57
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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.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.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
m.8393C>T rs1556423442

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