CNOT6[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2331699	NM_001370472.1(CNOT6):c.122G>A (p.Arg41Lys)	CNOT6 (R41K)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2343664	NM_001370472.1(CNOT6):c.260G>A (p.Arg87His)	CNOT6 (R87H)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2271667	NM_001370472.1(CNOT6):c.302A>T (p.Glu101Val)	CNOT6 (E101V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2302724	NM_001370472.1(CNOT6):c.353A>G (p.Lys118Arg)	CNOT6 (K118R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2600288	NM_001370472.1(CNOT6):c.557C>T (p.Thr186Ile)	CNOT6 (T186I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2558658	NM_001370472.1(CNOT6):c.619T>C (p.Tyr207His)	CNOT6 (Y112H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2479653	NM_001370472.1(CNOT6):c.1042C>T (p.Leu348Phe)	CNOT6 (L348F +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2551245	NM_001370472.1(CNOT6):c.1174C>T (p.Arg392Cys)	CNOT6 (R387C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2272387	NM_001370472.1(CNOT6):c.1378G>A (p.Gly460Arg)	CNOT6 (G365R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330683	NM_001370472.1(CNOT6):c.1420A>G (p.Ser474Gly)	CNOT6 (S469G +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance