List of variants in gene MT-ND4 reported as uncertain significance 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: 54

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND4):m.10776T>C	rs1603222966
NC_012920.1(MT-ND4):m.10785T>C	rs1603222970
NC_012920.1(MT-ND4):m.10791T>C	rs1603222973
NC_012920.1(MT-ND4):m.10857T>C	rs1603222990
NC_012920.1(MT-ND4):m.10863G>A	rs1603222992
NC_012920.1(MT-ND4):m.10911G>A	rs1603223016
NC_012920.1(MT-ND4):m.10913T>C	rs1603223017
NC_012920.1(MT-ND4):m.10915T>G	rs2857285
NC_012920.1(MT-ND4):m.10922A>G	rs1603223021
NC_012920.1(MT-ND4):m.10932C>T	rs1603223028
NC_012920.1(MT-ND4):m.11004G>A	rs1556423880
NC_012920.1(MT-ND4):m.11013C>A	rs879244441
NC_012920.1(MT-ND4):m.11043A>G	rs1603223072
NC_012920.1(MT-ND4):m.11069A>G	rs1603223091
NC_012920.1(MT-ND4):m.11090A>G	rs1603223101
NC_012920.1(MT-ND4):m.11111T>C	rs1603223109
NC_012920.1(MT-ND4):m.11120T>C	rs1603223116
NC_012920.1(MT-ND4):m.11139T>C	rs1603223126
NC_012920.1(MT-ND4):m.11144A>T	rs1603223129
NC_012920.1(MT-ND4):m.11157T>C	rs1603223138
NC_012920.1(MT-ND4):m.11223T>C	rs1603223170
NC_012920.1(MT-ND4):m.11232T>C	rs1603223180
NC_012920.1(MT-ND4):m.11246G>A	rs1603223192
NC_012920.1(MT-ND4):m.11289T>C	rs1603223215
NC_012920.1(MT-ND4):m.11301T>C	rs1603223221
NC_012920.1(MT-ND4):m.11360A>G	rs878928689
NC_012920.1(MT-ND4):m.11363G>A	rs1603223261
NC_012920.1(MT-ND4):m.11393C>T	rs1603223277
NC_012920.1(MT-ND4):m.11498A>G	rs1603223309
NC_012920.1(MT-ND4):m.11577G>A	rs1603223344
NC_012920.1(MT-ND4):m.11583T>C	rs1603223350
NC_012920.1(MT-ND4):m.11615A>G	rs1603223360
NC_012920.1(MT-ND4):m.11634G>A	rs1603223368
NC_012920.1(MT-ND4):m.11711G>A	rs1603223391
NC_012920.1(MT-ND4):m.11733T>C	rs1603223397
NC_012920.1(MT-ND4):m.11781T>C	rs1603223410
NC_012920.1(MT-ND4):m.11792T>G	rs1603223415
NC_012920.1(MT-ND4):m.11825G>A	rs879083692
NC_012920.1(MT-ND4):m.11906G>A	rs1603223460
NC_012920.1(MT-ND4):m.11913C>T	rs1603223463
NC_012920.1(MT-ND4):m.11931T>C	rs1603223474
NC_012920.1(MT-ND4):m.11964T>G	rs1603223491
NC_012920.1(MT-ND4):m.11978T>A	rs1603223502
NC_012920.1(MT-ND4):m.11981C>T	rs386829143
NC_012920.1(MT-ND4):m.11990T>C	rs1603223505
NC_012920.1(MT-ND4):m.12011T>G	rs386829144
NC_012920.1(MT-ND4):m.12013A>G	rs1057516067
NC_012920.1(MT-ND4):m.12018C>G	rs1057516068
NC_012920.1(MT-ND4):m.12031C>A	rs1603223519
NC_012920.1(MT-ND4):m.12040A>T	rs1603223523
NC_012920.1(MT-ND4):m.12054G>A	rs1603223526
NC_012920.1(MT-ND4):m.12117T>C	rs1603223549
NC_012920.1(MT-ND4):m.12122A>G	rs1603223553
NC_012920.1(MT-ND4):m.12128T>C	rs1603223557

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