ClinVar Miner

List of variants studied for Mitochondrial complex 1 deficiency, nuclear type 22 by OMIM

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_004544.4(NDUFA10):c.1A>G (p.Met1Val) rs387906872 0.00001
NM_004544.4(NDUFA10):c.384_385insAAT (p.Ser128_Tyr129insAsn) rs1057519415
NM_004544.4(NDUFA10):c.425A>G (p.Gln142Arg) rs387906873
NM_004544.4(NDUFA10):c.881T>C (p.Leu294Pro) rs1057519414

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