List of variants in gene NDUFA11 studied for Mitochondrial complex I deficiency, nuclear type 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_175614.5(NDUFA11):c.311G>T (p.Arg104Leu)	rs199842745	0.00042
NM_175614.5(NDUFA11):c.*59C>G	rs191571307	0.00033
NM_175614.5(NDUFA11):c.138G>A (p.Pro46=)	rs138889960	0.00029
NM_175614.4(NDUFA11):c.-282T>C	rs779432735	0.00006
NM_175614.5(NDUFA11):c.*63G>A	rs749166288	0.00006
NM_175614.5(NDUFA11):c.205G>A (p.Val69Met)	rs774174896	0.00006
NM_175614.4(NDUFA11):c.-300G>A	rs563822139	0.00004
NM_175614.5(NDUFA11):c.288C>T (p.Ala96=)	rs941748424	0.00002
NM_175614.5(NDUFA11):c.345C>T (p.Cys115=)	rs536499962	0.00001
NM_175614.5(NDUFA11):c.*55G>C	rs771648754
NM_175614.5(NDUFA11):c.104C>G (p.Thr35Ser)	rs2057614252
NM_175614.5(NDUFA11):c.233C>T (p.Ala78Val)	rs886054647
NM_175614.5(NDUFA11):c.234C>T (p.Ala78=)	rs1345378776

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