ClinVar Miner

List of variants in gene NDUFA10 reported as uncertain significance for Leigh syndrome

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Gene type:
ClinVar version:
Total variants: 116
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HGVS dbSNP gnomAD frequency
NM_004544.3(NDUFA10):c.-92C>T rs559797625 0.00474
NM_004544.3(NDUFA10):c.-93G>T rs577432343 0.00460
NM_004544.4(NDUFA10):c.*925C>G rs149563558 0.00292
NM_004544.4(NDUFA10):c.*1943A>G rs148829605 0.00283
NM_004544.4(NDUFA10):c.*546G>A rs192485848 0.00242
NM_004544.4(NDUFA10):c.*372C>T rs143693330 0.00222
NM_004544.4(NDUFA10):c.*632G>A rs189306598 0.00206
NM_004544.4(NDUFA10):c.*1161C>T rs184925264 0.00194
NM_004544.4(NDUFA10):c.*3141C>T rs144864637 0.00185
NM_004544.4(NDUFA10):c.548-9A>G rs147876332 0.00172
NM_004544.4(NDUFA10):c.*2242T>C rs111969519 0.00159
NM_004544.4(NDUFA10):c.*1198G>A rs143353868 0.00145
NM_004544.4(NDUFA10):c.*1879G>A rs143421241 0.00131
NM_004544.4(NDUFA10):c.*1915G>A rs144590599 0.00114
NM_004544.4(NDUFA10):c.*3095A>G rs576198967 0.00094
NM_004544.4(NDUFA10):c.*2659A>C rs559550890 0.00092
NM_004544.4(NDUFA10):c.*3347C>T rs537694779 0.00072
NM_004544.4(NDUFA10):c.*1303C>T rs575940810 0.00063
NM_004544.4(NDUFA10):c.*2297T>G rs773090030 0.00061
NM_004544.4(NDUFA10):c.*1482C>G rs557576958 0.00052
NM_004544.4(NDUFA10):c.*2149C>T rs570872300 0.00044
NM_004544.4(NDUFA10):c.*1992C>T rs373034894 0.00036
NM_004544.3(NDUFA10):c.-87A>C rs886055827 0.00031
NM_004544.4(NDUFA10):c.*1245G>A rs187916829 0.00024
NM_004544.4(NDUFA10):c.*2685C>A rs114807372 0.00024
NM_004544.4(NDUFA10):c.*1206G>A rs192203978 0.00021
NM_004544.4(NDUFA10):c.*389C>T rs539829771 0.00018
NM_004544.4(NDUFA10):c.749+11C>T rs200760509 0.00015
NM_004544.4(NDUFA10):c.*1057T>G rs541016943 0.00013
NM_004544.4(NDUFA10):c.*2111G>A rs752139055 0.00011
NM_004544.4(NDUFA10):c.*3409G>A rs146483651 0.00011
NM_004544.4(NDUFA10):c.*3067C>T rs564992184 0.00010
NM_004544.4(NDUFA10):c.354C>T (p.Tyr118=) rs118106981 0.00010
NM_004544.4(NDUFA10):c.*2649G>A rs886055815 0.00009
NM_004544.4(NDUFA10):c.*765C>T rs144208727 0.00009
NM_004544.4(NDUFA10):c.*1214C>T rs546735567 0.00008
NM_004544.4(NDUFA10):c.*2900G>A rs752124492 0.00008
NM_004544.4(NDUFA10):c.*3205G>A rs886055811 0.00006
NM_004544.4(NDUFA10):c.*361A>G rs778261754 0.00006
NM_004544.4(NDUFA10):c.41C>G (p.Ser14Cys) rs928084265 0.00006
NM_004544.4(NDUFA10):c.*1486C>T rs746931112 0.00005
NM_004544.4(NDUFA10):c.*2455C>G rs756778773 0.00005
NM_004544.4(NDUFA10):c.*1124C>T rs754187471 0.00004
NM_004544.4(NDUFA10):c.*3557G>A rs149933652 0.00004
NM_004544.4(NDUFA10):c.529G>A (p.Gly177Arg) rs759587515 0.00004
NM_004544.4(NDUFA10):c.549T>C (p.Cys183=) rs149783296 0.00004
NM_004544.4(NDUFA10):c.*1011A>G rs575477219 0.00003
NM_004544.4(NDUFA10):c.*1594G>A rs773071160 0.00003
NM_004544.4(NDUFA10):c.*2136T>C rs943989946 0.00003
NM_004544.4(NDUFA10):c.*2648C>T rs953906857 0.00003
NM_004544.4(NDUFA10):c.*3098A>T rs886055813 0.00003
NM_004544.4(NDUFA10):c.*489A>G rs886055824 0.00003
NM_004544.4(NDUFA10):c.865C>T (p.Arg289Cys) rs762669820 0.00003
NM_004544.4(NDUFA10):c.*1665C>A rs1314058965 0.00002
NM_004544.4(NDUFA10):c.*2382C>A rs1289543938 0.00002
NM_004544.4(NDUFA10):c.*3113G>A rs886055812 0.00002
NM_004544.4(NDUFA10):c.*861C>G rs551167199 0.00002
NM_004544.4(NDUFA10):c.1000-3C>G rs199648872 0.00002
NM_004544.4(NDUFA10):c.363G>A (p.Pro121=) rs749199433 0.00002
NM_004544.4(NDUFA10):c.925A>G (p.Ser309Gly) rs1222086753 0.00002
NM_004544.4(NDUFA10):c.*105G>A rs886055825 0.00001
NM_004544.4(NDUFA10):c.*1262C>T rs759194775 0.00001
NM_004544.4(NDUFA10):c.*1709T>C rs562457080 0.00001
NM_004544.4(NDUFA10):c.*1884G>C rs886055820 0.00001
NM_004544.4(NDUFA10):c.*1927G>C rs1227609332 0.00001
NM_004544.4(NDUFA10):c.*2079A>G rs1574808891 0.00001
NM_004544.4(NDUFA10):c.*2192T>A rs886055817 0.00001
NM_004544.4(NDUFA10):c.*2350G>A rs1218747092 0.00001
NM_004544.4(NDUFA10):c.*3143C>T rs1357789210 0.00001
NM_004544.4(NDUFA10):c.*3711A>G rs1466622883 0.00001
NM_004544.4(NDUFA10):c.*445C>G rs563264912 0.00001
NM_004544.4(NDUFA10):c.*732T>G rs1349086163 0.00001
NM_004544.4(NDUFA10):c.*804T>C rs1422021026 0.00001
NM_004544.4(NDUFA10):c.*857G>C rs1303822860 0.00001
NM_004544.4(NDUFA10):c.1000-12358G>A rs1265529467 0.00001
NM_004544.4(NDUFA10):c.1010G>A (p.Arg337His) rs201449418 0.00001
NM_004544.4(NDUFA10):c.460+5A>G rs1158773739 0.00001
NM_004544.4(NDUFA10):c.63C>G (p.Gly21=) rs980893132 0.00001
NM_004544.4(NDUFA10):c.985C>T (p.His329Tyr) rs1188020120 0.00001
NM_004544.4(NDUFA10):c.*1047T>C rs1694787943
NM_004544.4(NDUFA10):c.*1129G>A rs886055822
NM_004544.4(NDUFA10):c.*1212T>C rs886055821
NM_004544.4(NDUFA10):c.*1391C>T rs552149779
NM_004544.4(NDUFA10):c.*1586A>G rs1483288404
NM_004544.4(NDUFA10):c.*1702G>A rs1694755462
NM_004544.4(NDUFA10):c.*1894_*1914delinsGGG rs886055819
NM_004544.4(NDUFA10):c.*2009G>C rs370309206
NM_004544.4(NDUFA10):c.*2042A>C rs886055818
NM_004544.4(NDUFA10):c.*2046T>C rs1694740787
NM_004544.4(NDUFA10):c.*2397A>G rs886055816
NM_004544.4(NDUFA10):c.*2838C>A rs532456176
NM_004544.4(NDUFA10):c.*2997G>A rs886055814
NM_004544.4(NDUFA10):c.*3009T>C rs1694711139
NM_004544.4(NDUFA10):c.*3052G>A rs1003876097
NM_004544.4(NDUFA10):c.*3175T>G rs1694704488
NM_004544.4(NDUFA10):c.*3301C>T rs1694700570
NM_004544.4(NDUFA10):c.*3403A>G rs1574807018
NM_004544.4(NDUFA10):c.*3408T>C rs886055810
NM_004544.4(NDUFA10):c.*3456T>G rs1694694826
NM_004544.4(NDUFA10):c.*3490G>C rs1694693520
NM_004544.4(NDUFA10):c.*3724G>A rs1694684016
NM_004544.4(NDUFA10):c.*412A>G rs546052985
NM_004544.4(NDUFA10):c.*435A>G rs1054245819
NM_004544.4(NDUFA10):c.*548G>C rs1694810369
NM_004544.4(NDUFA10):c.*740C>T rs886055823
NM_004544.4(NDUFA10):c.-34C>T rs920826583
NM_004544.4(NDUFA10):c.-36C>T rs886055826
NM_004544.4(NDUFA10):c.110G>T (p.Arg37Leu) rs558134843
NM_004544.4(NDUFA10):c.270G>A (p.Gly90=) rs770747594
NM_004544.4(NDUFA10):c.29C>T (p.Ala10Val) rs1258770997
NM_004544.4(NDUFA10):c.484T>C (p.Ser162Pro) rs1559403435
NM_004544.4(NDUFA10):c.558C>T (p.His186=) rs1407750102
NM_004544.4(NDUFA10):c.604dup (p.His202fs) rs746019378
NM_004544.4(NDUFA10):c.630C>T (p.Pro210=) rs148656779
NM_004544.4(NDUFA10):c.749+5G>A rs1697147446
NM_004544.4(NDUFA10):c.994A>G (p.Arg332Gly) rs758042753

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