"MRPL10-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059980	NM_145255.4(MRPL10):c.373G>A (p.Val125Ile)	MRPL10 (V125I +1 more)	Single nucleotide variant (missense variant +1 more)	MRPL10-related disorder	GBenign
Select item 3039902	NM_145255.4(MRPL10):c.192C>T (p.Cys64=)	MRPL10	Single nucleotide variant (synonymous variant +1 more)	MRPL10-related disorder	GLikely benign
Select item 3052044	NM_145255.4(MRPL10):c.87C>T (p.Gly29=)	MRPL10	Single nucleotide variant (synonymous variant +1 more)	MRPL10-related disorder	GLikely benign

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