List of variants in gene MRPL3 reported as uncertain significance for Combined oxidative phosphorylation defect type 9

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_007208.4(MRPL3):c.862T>C (p.Ser288Pro)	rs143788120	0.00027
NM_007208.4(MRPL3):c.379T>C (p.Cys127Arg)
NM_007208.4(MRPL3):c.793T>C (p.Tyr265His)

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