List of variants reported as likely pathogenic for Mitochondrial complex 1 deficiency, nuclear type 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_024407.5(NDUFS7):c.364G>A (p.Val122Met)	rs104894705	0.00009
NM_024407.5(NDUFS7):c.339_348del (p.Arg115fs)
NM_024407.5(NDUFS7):c.343_352dup (p.Asp118fs)
NM_024407.5(NDUFS7):c.345_354del (p.Gln116fs)
NM_024407.5(NDUFS7):c.408+1G>C

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