ClinVar Miner

List of variants in gene NDUFA10 studied for Leigh syndrome

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_001322019.1(NDUFA10):c.-87A>C rs886055827
NM_001322019.1(NDUFA10):c.-92C>T rs559797625
NM_001322019.1(NDUFA10):c.-93G>T rs577432343
NM_004544.4(NDUFA10):c.*1011A>G rs575477219
NM_004544.4(NDUFA10):c.*105G>A rs886055825
NM_004544.4(NDUFA10):c.*1129G>A rs886055822
NM_004544.4(NDUFA10):c.*1189C>T rs66534347
NM_004544.4(NDUFA10):c.*1212T>C rs886055821
NM_004544.4(NDUFA10):c.*1214C>T rs546735567
NM_004544.4(NDUFA10):c.*1229C>G rs55998047
NM_004544.4(NDUFA10):c.*1262C>T rs759194775
NM_004544.4(NDUFA10):c.*1884G>C rs886055820
NM_004544.4(NDUFA10):c.*1894_*1914delinsGGG rs886055819
NM_004544.4(NDUFA10):c.*1915G>A rs144590599
NM_004544.4(NDUFA10):c.*1923_*1924insA rs138899326
NM_004544.4(NDUFA10):c.*1957G>A rs4854069
NM_004544.4(NDUFA10):c.*2042A>C rs886055818
NM_004544.4(NDUFA10):c.*2111G>A rs752139055
NM_004544.4(NDUFA10):c.*2149C>T rs570872300
NM_004544.4(NDUFA10):c.*2192T>A rs886055817
NM_004544.4(NDUFA10):c.*2297T>G rs773090030
NM_004544.4(NDUFA10):c.*2309G>A rs1132778
NM_004544.4(NDUFA10):c.*2397A>G rs886055816
NM_004544.4(NDUFA10):c.*2495C>T rs78395168
NM_004544.4(NDUFA10):c.*2602C>T rs58261980
NM_004544.4(NDUFA10):c.*2649G>A rs886055815
NM_004544.4(NDUFA10):c.*2685C>A rs114807372
NM_004544.4(NDUFA10):c.*2997G>A rs886055814
NM_004544.4(NDUFA10):c.*3067C>T rs564992184
NM_004544.4(NDUFA10):c.*3075T>G rs7588974
NM_004544.4(NDUFA10):c.*308C>T rs8369
NM_004544.4(NDUFA10):c.*3098A>T rs886055813
NM_004544.4(NDUFA10):c.*3113G>A rs886055812
NM_004544.4(NDUFA10):c.*3141C>T rs144864637
NM_004544.4(NDUFA10):c.*3204C>T rs34277046
NM_004544.4(NDUFA10):c.*3205G>A rs886055811
NM_004544.4(NDUFA10):c.*3349G>A rs77216981
NM_004544.4(NDUFA10):c.*3408T>C rs886055810
NM_004544.4(NDUFA10):c.*3450G>A rs7573892
NM_004544.4(NDUFA10):c.*3557G>A rs149933652
NM_004544.4(NDUFA10):c.*361A>G rs778261754
NM_004544.4(NDUFA10):c.*389C>T rs539829771
NM_004544.4(NDUFA10):c.*407C>T rs74614612
NM_004544.4(NDUFA10):c.*412A>G rs546052985
NM_004544.4(NDUFA10):c.*414G>A rs13424612
NM_004544.4(NDUFA10):c.*438C>T rs13396556
NM_004544.4(NDUFA10):c.*489A>G rs886055824
NM_004544.4(NDUFA10):c.*546G>A rs192485848
NM_004544.4(NDUFA10):c.*631C>T rs10933622
NM_004544.4(NDUFA10):c.*647C>T rs116254382
NM_004544.4(NDUFA10):c.*740C>T rs886055823
NM_004544.4(NDUFA10):c.*925C>G rs149563558
NM_004544.4(NDUFA10):c.-36C>T rs886055826
NM_004544.4(NDUFA10):c.1000-3C>G rs199648872
NM_004544.4(NDUFA10):c.1000-5del rs138479490
NM_004544.4(NDUFA10):c.105A>G (p.Lys35=) rs2083411
NM_004544.4(NDUFA10):c.24G>A (p.Leu8=) rs113012830
NM_004544.4(NDUFA10):c.270G>A (p.Gly90=) rs770747594
NM_004544.4(NDUFA10):c.548-9A>G rs147876332
NM_004544.4(NDUFA10):c.549T>C (p.Cys183=) rs149783296
NM_004544.4(NDUFA10):c.5C>G (p.Ala2Gly) rs11541494
NM_004544.4(NDUFA10):c.749+11C>T rs200760509
NM_004544.4(NDUFA10):c.771A>G (p.Gln257=) rs13848
NM_004544.4(NDUFA10):c.865C>T (p.Arg289Cys) rs762669820

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