"PreventionGenetics, part of Exact Sciences"[submitter] AND "AGMO"[gen - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 434105	NM_001004320.2(AGMO):c.1263+8del	AGMO	Deletion (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2633128	NM_001004320.2(AGMO):c.1234C>A (p.Leu412Ile)	AGMO (L412I)	Single nucleotide variant (missense variant)	AGMO-related disorder	GUncertain significance
Select item 3033422	NM_001004320.2(AGMO):c.1224C>T (p.His408=)	AGMO	Single nucleotide variant (synonymous variant)	AGMO-related disorder	GLikely benign
Select item 3038022	NM_001004320.2(AGMO):c.1183C>G (p.Leu395Val)	AGMO (L395V)	Single nucleotide variant (missense variant)	AGMO-related disorder	GBenign
Select item 3045580	NM_001004320.2(AGMO):c.1181C>G (p.Thr394Ser)	AGMO (T394S)	Single nucleotide variant (missense variant)	AGMO-related disorder	GLikely benign
Select item 3039486	NM_001004320.2(AGMO):c.1074+10A>G	AGMO	Single nucleotide variant (intron variant)	AGMO-related disorder	GLikely benign
Select item 3044878	NM_001004320.2(AGMO):c.904C>T (p.Pro302Ser)	AGMO (P302S)	Single nucleotide variant (missense variant)	AGMO-related disorder	GUncertain significance
Select item 3040600	NM_001004320.2(AGMO):c.851C>T (p.Thr284Ile)	AGMO (T284I)	Single nucleotide variant (missense variant)	AGMO-related disorder	GBenign
Select item 3056029	NM_001004320.2(AGMO):c.839C>A (p.Ser280Tyr)	AGMO (S280Y)	Single nucleotide variant (missense variant)	AGMO-related disorder	GBenign
Select item 2637247	NM_001004320.2(AGMO):c.790C>T (p.Pro264Ser)	AGMO (P264S)	Single nucleotide variant (missense variant)	AGMO-related disorder	GUncertain significance
Select item 1236929	NM_001004320.2(AGMO):c.606A>G (p.Thr202=)	AGMO	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 790038	NM_001004320.2(AGMO):c.429C>T (p.Ala143=)	AGMO	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 716356	NM_001004320.2(AGMO):c.92A>G (p.Gln31Arg)	AGMO (Q31R)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign