ClinVar Miner

List of variants in gene MT-ATP8 reported as benign for Leigh syndrome

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ATP8):m.8381A>G rs1603221438
NC_012920.1(MT-ATP8):m.8387G>A rs1556423439
NC_012920.1(MT-ATP8):m.8388T>C rs879199176
NC_012920.1(MT-ATP8):m.8396A>G rs1603221454
NC_012920.1(MT-ATP8):m.8400T>C rs1603221459
NC_012920.1(MT-ATP8):m.8406C>T rs1556423448
NC_012920.1(MT-ATP8):m.8414C>T rs28358884
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.8433T>C rs1603221480
NC_012920.1(MT-ATP8):m.8435A>G rs1603221481
NC_012920.1(MT-ATP8):m.8448T>C rs879056797
NC_012920.1(MT-ATP8):m.8454A>G rs1603221488
NC_012920.1(MT-ATP8):m.8460A>G rs1116906
NC_012920.1(MT-ATP8):m.8462T>C rs1603221496
NC_012920.1(MT-ATP8):m.8463A>G rs1603221498
NC_012920.1(MT-ATP8):m.8472C>T rs879209186
NC_012920.1(MT-ATP8):m.8477T>C rs1603221517
NC_012920.1(MT-ATP8):m.8478C>T rs201902227
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.8504T>C rs1603221542
NC_012920.1(MT-ATP8):m.8508A>G rs1603221548
NC_012920.1(MT-ATP8):m.8519G>A rs878853091
NC_012920.1(MT-ATP8):m.8522C>T rs1603221562
m.8393C>T rs1556423442

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