"Ambry Genetics"[submitter] AND "LOC129996445"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296067	NM_018141.4(MRPS10):c.41T>C (p.Leu14Pro)	LOC129996445, MRPS10 (L14P)	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
Select item 2291185	NM_018141.4(MRPS10):c.5C>T (p.Ala2Val)	LOC129996445, MRPS10 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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ClinVar