"Ambry Genetics"[submitter] AND "MRPS10"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2376180	NM_018141.4(MRPS10):c.593A>C (p.Glu198Ala)	MRPS10 (E198A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456141	NM_018141.4(MRPS10):c.559C>T (p.Pro187Ser)	MRPS10 (P187S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296068	NM_018141.4(MRPS10):c.502G>A (p.Val168Ile)	MRPS10 (V168I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208539	NM_018141.4(MRPS10):c.474A>T (p.Glu158Asp)	MRPS10 (E158D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355249	NM_018141.4(MRPS10):c.316A>G (p.Ile106Val)	MRPS10 (I106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208534	NM_018141.4(MRPS10):c.256G>A (p.Ala86Thr)	MRPS10 (A86T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208525	NM_018141.4(MRPS10):c.230C>T (p.Ser77Leu)	MRPS10 (S77L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395926	NM_018141.4(MRPS10):c.108G>C (p.Leu36Phe)	MRPS10 (L36F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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