ClinVar Miner

List of variants in gene MT-ATP6 reported as uncertain significance for Leigh syndrome

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Gene type:
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Total variants: 86
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ATP6):m.8576T>C rs1603221596
NC_012920.1(MT-ATP6):m.8591T>C rs1603221609
NC_012920.1(MT-ATP6):m.8593A>G rs1603221612
NC_012920.1(MT-ATP6):m.8599C>A rs1603221623
NC_012920.1(MT-ATP6):m.8605C>T rs1603221630
NC_012920.1(MT-ATP6):m.8609C>T rs1603221634
NC_012920.1(MT-ATP6):m.8612T>C rs1603221635
NC_012920.1(MT-ATP6):m.8615T>C rs1603221637
NC_012920.1(MT-ATP6):m.8623A>C rs1603221645
NC_012920.1(MT-ATP6):m.8623A>T rs1603221645
NC_012920.1(MT-ATP6):m.8641A>G rs1603221662
NC_012920.1(MT-ATP6):m.8642A>C rs1603221663
NC_012920.1(MT-ATP6):m.8697G>T rs879233543
NC_012920.1(MT-ATP6):m.8699T>C rs1603221710
NC_012920.1(MT-ATP6):m.8700A>T rs1603221711
NC_012920.1(MT-ATP6):m.8714C>T rs1603221724
NC_012920.1(MT-ATP6):m.8720G>A rs1603221728
NC_012920.1(MT-ATP6):m.8720G>C rs1603221728
NC_012920.1(MT-ATP6):m.8722C>T rs1603221733
NC_012920.1(MT-ATP6):m.8728T>C rs1603221742
NC_012920.1(MT-ATP6):m.8731T>A rs1603221746
NC_012920.1(MT-ATP6):m.8735T>C rs1603221752
NC_012920.1(MT-ATP6):m.8737A>G rs1603221754
NC_012920.1(MT-ATP6):m.8744T>C rs1603221756
NC_012920.1(MT-ATP6):m.8746T>C rs1603221761
NC_012920.1(MT-ATP6):m.8761A>C rs1603221776
NC_012920.1(MT-ATP6):m.8782G>A rs1603221801
NC_012920.1(MT-ATP6):m.8785C>G rs1603221807
NC_012920.1(MT-ATP6):m.8785C>T rs1603221807
NC_012920.1(MT-ATP6):m.8789T>C rs1603221811
NC_012920.1(MT-ATP6):m.8800T>G rs1569484239
NC_012920.1(MT-ATP6):m.8812A>T rs1556423543
NC_012920.1(MT-ATP6):m.8821T>C rs1603221825
NC_012920.1(MT-ATP6):m.8824A>G rs1603221827
NC_012920.1(MT-ATP6):m.8825T>C rs1603221830
NC_012920.1(MT-ATP6):m.8840C>T rs1603221837
NC_012920.1(MT-ATP6):m.8844C>A rs1603221840
NC_012920.1(MT-ATP6):m.8863G>A rs1603221852
NC_012920.1(MT-ATP6):m.8868T>A rs1556423556
NC_012920.1(MT-ATP6):m.8873G>C rs1603221864
NC_012920.1(MT-ATP6):m.8879G>A rs1603221870
NC_012920.1(MT-ATP6):m.8906A>C rs1603221897
NC_012920.1(MT-ATP6):m.8920G>A rs28406348
NC_012920.1(MT-ATP6):m.8921G>A rs2298008
NC_012920.1(MT-ATP6):m.8933C>T rs1603221918
NC_012920.1(MT-ATP6):m.8935C>T rs28377547
NC_012920.1(MT-ATP6):m.8936T>C rs1603221920
NC_012920.1(MT-ATP6):m.8941C>T rs1603221928
NC_012920.1(MT-ATP6):m.8951T>C rs1603221934
NC_012920.1(MT-ATP6):m.8953A>G rs1603221936
NC_012920.1(MT-ATP6):m.8954T>C rs1556423576
NC_012920.1(MT-ATP6):m.8959G>A rs1603221944
NC_012920.1(MT-ATP6):m.8972T>C rs1603221948
NC_012920.1(MT-ATP6):m.9005T>C rs1603221971
NC_012920.1(MT-ATP6):m.9014A>G rs1603221980
NC_012920.1(MT-ATP6):m.9019A>G rs1603221982
NC_012920.1(MT-ATP6):m.9026G>A rs1603221987
NC_012920.1(MT-ATP6):m.9028C>T rs1603221990
NC_012920.1(MT-ATP6):m.9029A>G rs1603221991
NC_012920.1(MT-ATP6):m.9035T>C rs1603222000
NC_012920.1(MT-ATP6):m.9047T>C rs1603222008
NC_012920.1(MT-ATP6):m.9058A>C rs1556423599
NC_012920.1(MT-ATP6):m.9070T>C rs879190502
NC_012920.1(MT-ATP6):m.9073A>C rs1556423603
NC_012920.1(MT-ATP6):m.9082C>T rs1603222043
NC_012920.1(MT-ATP6):m.9085C>A rs1603222048
NC_012920.1(MT-ATP6):m.9086C>T rs1603222049
NC_012920.1(MT-ATP6):m.9099C>A rs1603222065
NC_012920.1(MT-ATP6):m.9104T>C rs1603222079
NC_012920.1(MT-ATP6):m.9106A>G rs1603222082
NC_012920.1(MT-ATP6):m.9122T>G rs1603222104
NC_012920.1(MT-ATP6):m.9125C>T rs1603222109
NC_012920.1(MT-ATP6):m.9133G>A rs1603222118
NC_012920.1(MT-ATP6):m.9140C>T rs878972895
NC_012920.1(MT-ATP6):m.9160T>C rs1603222140
NC_012920.1(MT-ATP6):m.9167T>C rs1603222143
NC_012920.1(MT-ATP6):m.9169A>G rs1603222145
NC_012920.1(MT-ATP6):m.9170C>T rs1603222148
NC_012920.1(MT-ATP6):m.9179T>C rs1603222150
NC_012920.1(MT-ATP6):m.9188A>G rs1603222161
NC_012920.1(MT-ATP6):m.9194A>G rs1603222162
NC_012920.1(MT-ATP6):m.9202A>G rs1603222169
NC_012920.1(MT-ATP6):m.9205T>C rs1603222171
NC_012920.1:m.8651T>C rs1556423512
NC_012920.1:m.8686T>C rs1569484231
NC_012920.1:m.9166T>C rs1057516063

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