ClinVar Miner

List of variants in gene NDUFA10 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_004544.4(NDUFA10):c.*1923_*1924insA rs138899326 0.11754
NM_004544.4(NDUFA10):c.*3075T>G rs7588974 0.03737
NM_004544.4(NDUFA10):c.*3349G>A rs77216981 0.02367
NM_004544.4(NDUFA10):c.*2511C>T rs74540213 0.01512
NM_004544.4(NDUFA10):c.*1217A>G rs116403651 0.01210
NM_004544.4(NDUFA10):c.*1878C>T rs80067639 0.01081
NM_004544.4(NDUFA10):c.*3544C>T rs114944621 0.01013
NM_004544.4(NDUFA10):c.194A>G (p.Asn65Ser) rs35715497 0.00925
NM_004544.4(NDUFA10):c.*407C>T rs74614612 0.00847
NM_004544.4(NDUFA10):c.*647C>T rs116254382 0.00794
NM_004544.4(NDUFA10):c.*1453G>A rs192964209 0.00706
NM_004544.4(NDUFA10):c.712G>A (p.Glu238Lys) rs35462421 0.00570
NM_004544.4(NDUFA10):c.*1382C>T rs111337344 0.00263
NM_004544.4(NDUFA10):c.-38T>G rs374970309 0.00206
NM_004544.4(NDUFA10):c.*2202C>T rs77614498 0.00120
NM_004544.4(NDUFA10):c.*2495C>T rs78395168 0.00119
NM_004544.4(NDUFA10):c.*679A>G rs374065697 0.00027
NM_004544.4(NDUFA10):c.*183C>T rs112660586 0.00023
NM_004544.4(NDUFA10):c.404T>C (p.Leu135Ser) rs140776586 0.00020
NM_004544.4(NDUFA10):c.*428C>T rs557106858 0.00004
NM_004544.4(NDUFA10):c.*1930C>G rs535714073 0.00001
NM_004544.4(NDUFA10):c.1000-5del rs138479490

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