"Ambry Genetics"[submitter] AND "CNOT10-AS1"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2480358	NM_015442.3(CNOT10):c.1313A>G (p.Gln438Arg)	CNOT10, CNOT10-AS1 (Q498R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2459904	NM_015442.3(CNOT10):c.1387A>G (p.Ile463Val)	CNOT10, CNOT10-AS1 (I523V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2329544	NM_015442.3(CNOT10):c.1517G>T (p.Ser506Ile)	CNOT10, CNOT10-AS1 (S566I +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2383993	NM_015442.3(CNOT10):c.1543A>C (p.Ile515Leu)	CNOT10-AS1, CNOT10 (I514L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2363308	NM_015442.3(CNOT10):c.1543A>G (p.Ile515Val)	CNOT10, CNOT10-AS1 (I575V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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