ClinVar for Gene (Select 4514) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3027421	NC_012920.1(MT-CO3):m.9540T>C	MT-CO3	Single nucleotide variant	Venous thromboembolism	GBenign
Select item 1708973	NC_012920.1(MT-CO3):m.9247G>C	MT-CO3	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GUncertain significance
Select item 693258	NC_012920.1(MT-CO3):m.9987T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693257	NC_012920.1(MT-CO3):m.9984G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693256	NC_012920.1(MT-CO3):m.9981T>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693255	NC_012920.1(MT-CO3):m.9972A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693254	NC_012920.1(MT-CO3):m.9967T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693253	NC_012920.1(MT-CO3):m.9966G>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693252	NC_012920.1(MT-CO3):m.9957T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693251	NC_012920.1(MT-CO3):m.9948G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693250	NC_012920.1(MT-CO3):m.9939G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693249	NC_012920.1(MT-CO3):m.9922C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693248	NC_012920.1(MT-CO3):m.9921G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693247	NC_012920.1(MT-CO3):m.9911C>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693246	NC_012920.1(MT-CO3):m.9909T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693245	NC_012920.1(MT-CO3):m.9903T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693244	NC_012920.1(MT-CO3):m.9868G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693243	NC_012920.1(MT-CO3):m.9862T>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693242	NC_012920.1(MT-CO3):m.9856T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693241	NC_012920.1(MT-CO3):m.9855A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693240	NC_012920.1(MT-CO3):m.9852A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693239	NC_012920.1(MT-CO3):m.9844C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693238	NC_012920.1(MT-CO3):m.9843A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693237	NC_012920.1(MT-CO3):m.9838G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693236	NC_012920.1(MT-CO3):m.9837G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693235	NC_012920.1(MT-CO3):m.9828G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693234	NC_012920.1(MT-CO3):m.9822C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693233	NC_012920.1(MT-CO3):m.9820G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693232	NC_012920.1(MT-CO3):m.9819G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693231	NC_012920.1(MT-CO3):m.9813T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693230	NC_012920.1(MT-CO3):m.9804G>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693229	NC_012920.1(MT-CO3):m.9804G>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693228	NC_012920.1(MT-CO3):m.9802T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693227	NC_012920.1(MT-CO3):m.9801G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693226	NC_012920.1(MT-CO3):m.9786G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693225	NC_012920.1(MT-CO3):m.9777G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693224	NC_012920.1(MT-CO3):m.9769T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693223	NC_012920.1(MT-CO3):m.9765A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693222	NC_012920.1(MT-CO3):m.9759C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693221	NC_012920.1(MT-CO3):m.9756T>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693220	NC_012920.1(MT-CO3):m.9754A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693219	NC_012920.1(MT-CO3):m.9753G>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693218	NC_012920.1(MT-CO3):m.9753G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693217	NC_012920.1(MT-CO3):m.9752C>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693216	NC_012920.1(MT-CO3):m.9751T>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693215	NC_012920.1(MT-CO3):m.9751T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693214	NC_012920.1(MT-CO3):m.9739C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693213	NC_012920.1(MT-CO3):m.9738G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693212	NC_012920.1(MT-CO3):m.9727C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693211	NC_012920.1(MT-CO3):m.9717C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693210	NC_012920.1(MT-CO3):m.9706T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693209	NC_012920.1(MT-CO3):m.9705A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693208	NC_012920.1(MT-CO3):m.9700T>C	MT-CO3	Single nucleotide variant	Mitochondrial complex IV deficiency, nuclear type 1 +1 more	GUncertain significance
Select item 693207	NC_012920.1(MT-CO3):m.9699A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693206	NC_012920.1(MT-CO3):m.9685T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693205	NC_012920.1(MT-CO3):m.9682T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693204	NC_012920.1(MT-CO3):m.9670A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693203	NC_012920.1(MT-CO3):m.9667A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693202	NC_012920.1(MT-CO3):m.9664A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693201	NC_012920.1(MT-CO3):m.9663G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693200	NC_012920.1(MT-CO3):m.9660A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693199	NC_012920.1(MT-CO3):m.9654A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693198	NC_012920.1(MT-CO3):m.9652A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693197	NC_012920.1(MT-CO3):m.9637T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693196	NC_012920.1(MT-CO3):m.9636A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693195	NC_012920.1(MT-CO3):m.9633T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693194	NC_012920.1(MT-CO3):m.9631T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693193	NC_012920.1(MT-CO3):m.9630G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693192	NC_012920.1(MT-CO3):m.9621G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693191	NC_012920.1(MT-CO3):m.9612G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693190	NC_012920.1(MT-CO3):m.9604A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693189	NC_012920.1(MT-CO3):m.9592T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693188	NC_012920.1(MT-CO3):m.9591G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693187	NC_012920.1(MT-CO3):m.9588G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693186	NC_012920.1(MT-CO3):m.9582C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693185	NC_012920.1(MT-CO3):m.9580A>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693184	NC_012920.1(MT-CO3):m.9577T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693183	NC_012920.1(MT-CO3):m.9571C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693182	NC_012920.1(MT-CO3):m.9564G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693181	NC_012920.1(MT-CO3):m.9549C>T	MT-CO3	Single nucleotide variant	Leigh syndrome +1 more	GUncertain significance
Select item 693180	NC_012920.1(MT-CO3):m.9531A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693179	NC_012920.1(MT-CO3):m.9525G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693178	NC_012920.1(MT-CO3):m.9508T>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693177	NC_012920.1(MT-CO3):m.9495T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693176	NC_012920.1(MT-CO3):m.9490C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693175	NC_012920.1(MT-CO3):m.9489G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693174	NC_012920.1(MT-CO3):m.9484T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693173	NC_012920.1(MT-CO3):m.9481T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693172	NC_012920.1(MT-CO3):m.9480T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693171	NC_012920.1(MT-CO3):m.9478T>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693170	NC_012920.1(MT-CO3):m.9477G>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693169	NC_012920.1(MT-CO3):m.9477G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693168	NC_012920.1(MT-CO3):m.9469C>T	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693167	NC_012920.1(MT-CO3):m.9468A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693166	NC_012920.1(MT-CO3):m.9456A>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693165	NC_012920.1(MT-CO3):m.9456A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693164	NC_012920.1(MT-CO3):m.9448A>G	MT-CO3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693163	NC_012920.1(MT-CO3):m.9445G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693162	NC_012920.1(MT-CO3):m.9439G>A	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 693161	NC_012920.1(MT-CO3):m.9405T>C	MT-CO3	Single nucleotide variant	Leigh syndrome	GUncertain significance

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