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

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559267	NM_002541.4(OGDH):c.39A>C (p.Pro13=)	OGDH	Single nucleotide variant (synonymous variant)	Oxoglutaricaciduria +2 more	GBenign/Likely benign
Select item 780042	NM_002541.4(OGDH):c.164C>T (p.Ser55Leu)	OGDH (S55L)	Single nucleotide variant (missense variant)	OGDH-related disorder +2 more	GBenign
Select item 3044784	NM_002541.4(OGDH):c.171T>C (p.Tyr57=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder	GLikely benign
Select item 559269	NM_002541.4(OGDH):c.396G>A (p.Ser132=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign
Select item 721330	NM_002541.4(OGDH):c.474C>T (p.Asp158=)	OGDH	Single nucleotide variant (synonymous variant +1 more)	Oxoglutaricaciduria +1 more	GLikely benign
Select item 3051775	NM_002541.4(OGDH):c.936-8C>T	OGDH	Single nucleotide variant (intron variant)	OGDH-related disorder	GLikely benign
Select item 1643526	NM_002541.4(OGDH):c.1032C>T (p.Ser344=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign/Likely benign
Select item 791078	NM_002541.4(OGDH):c.1188C>T (p.Gly396=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +2 more	GBenign/Likely benign
Select item 1598081	NM_002541.4(OGDH):c.1206+19C>A	OGDH (R409S)	Single nucleotide variant (missense variant +1 more)	OGDH-related disorder +1 more	GBenign/Likely benign
Select item 1650649	NM_002541.4(OGDH):c.1542C>T (p.Asn514=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GLikely benign
Select item 1087513	NM_002541.4(OGDH):c.1659T>C (p.Pro553=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GLikely benign
Select item 724706	NM_002541.4(OGDH):c.1830G>A (p.Thr610=)	OGDH	Single nucleotide variant (synonymous variant)	Oxoglutaricaciduria +1 more	GBenign/Likely benign
Select item 785215	NM_002541.4(OGDH):c.1857T>C (p.Asn619=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign
Select item 3054492	NM_002541.4(OGDH):c.1980G>A (p.Ala660=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder	GLikely benign
Select item 3048295	NM_002541.4(OGDH):c.2051+9del	OGDH	Deletion (intron variant)	OGDH-related disorder	GLikely benign
Select item 2046041	NM_002541.4(OGDH):c.2145G>A (p.Val715=)	OGDH	Single nucleotide variant (synonymous variant)	Oxoglutaricaciduria +1 more	GBenign/Likely benign
Select item 559272	NM_002541.4(OGDH):c.2784A>G (p.Thr928=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign
Select item 559273	NM_002541.4(OGDH):c.2973G>A (p.Ala991=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign
Select item 559274	NM_002541.4(OGDH):c.2988C>T (p.Thr996=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign
Select item 559275	NM_002541.4(OGDH):c.3052G>A (p.Val1018Ile)	OGDH (V1018I +2 more)	Single nucleotide variant (missense variant)	OGDH-related disorder +1 more	GBenign
Select item 559276	NM_002541.4(OGDH):c.3063C>T (p.Asn1021=)	OGDH	Single nucleotide variant (synonymous variant)	OGDH-related disorder +1 more	GBenign

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Items: 21