List of variants in gene combination MYCL, TRIT1 reported as uncertain significance for combined oxidative phosphorylation deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017646.6(TRIT1):c.16G>A (p.Ala6Thr)	rs138415849	0.00046
NM_017646.6(TRIT1):c.23G>C (p.Arg8Pro)
NM_017646.6(TRIT1):c.65C>T (p.Thr22Ile)

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