ClinVar Miner

List of variants reported as pathogenic for Mitochondrial complex I deficiency, nuclear type 1 by Baylor Genetics

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_199069.2(NDUFAF3):c.188dup (p.Tyr63Ter) rs756339822 0.00023
NM_007103.4(NDUFV1):c.1268C>T (p.Thr423Met) rs121913659 0.00004
NM_174889.5(NDUFAF2):c.114C>G (p.Tyr38Ter) rs199754807 0.00003
NM_002495.4(NDUFS4):c.99-1G>A rs376281345 0.00001
NM_002495.4(NDUFS4):c.221del (p.Thr74fs)
NM_002495.4(NDUFS4):c.350+1G>A rs1260453815
NM_002495.4(NDUFS4):c.393dup (p.Glu132fs)
NM_002495.4(NDUFS4):c.462del (p.Lys154fs) rs587776949
NM_018480.7(TMEM126B):c.320_321del (p.Tyr107fs) rs752316853

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