Related gene-specific medical variations for Gene (Select 55173) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656548	NM_018141.4(MRPS10):c.15A>G (p.Thr5=)	LOC129996445, MRPS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2291185	NM_018141.4(MRPS10):c.5C>T (p.Ala2Val)	LOC129996445, MRPS10 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274890	NM_018141.4(MRPS10):c.23G>C (p.Gly8Ala)	LOC129996445, MRPS10 (G8A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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