"Ambry Genetics"[submitter] AND "OGDH"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2481891	NM_002541.4(OGDH):c.71C>T (p.Ser24Leu)	OGDH (S24L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591714	NM_002541.4(OGDH):c.113G>A (p.Arg38Gln)	OGDH (R38Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204088	NM_002541.4(OGDH):c.130G>T (p.Val44Phe)	OGDH (V44F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204090	NM_002541.4(OGDH):c.161G>A (p.Ser54Asn)	OGDH (S54N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302198	NM_002541.4(OGDH):c.168C>A (p.Asn56Lys)	OGDH (N56K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204094	NM_002541.4(OGDH):c.552G>C (p.Lys184Asn)	OGDH (K180N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488531	NM_002541.4(OGDH):c.619A>T (p.Ile207Phe)	OGDH (I203F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540983	NM_002541.4(OGDH):c.679G>C (p.Asp227His)	OGDH (D238H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597220	NM_002541.4(OGDH):c.779G>A (p.Arg260Gln)	OGDH (R256Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302200	NM_002541.4(OGDH):c.808C>T (p.Arg270Trp)	OGDH (R266W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218587	NM_002541.4(OGDH):c.1171G>A (p.Glu391Lys)	OGDH (E402K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603192	NM_002541.4(OGDH):c.1183T>C (p.Cys395Arg)	OGDH (C406R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204089	NM_002541.4(OGDH):c.1396C>G (p.Arg466Gly)	OGDH (R477G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2054870	NM_002541.4(OGDH):c.1595A>G (p.Lys532Arg)	OGDH (K532R +2 more)	Single nucleotide variant (missense variant)	Oxoglutaricaciduria +1 more	GUncertain significance
Select item 2569151	NM_002541.4(OGDH):c.1813C>T (p.Pro605Ser)	OGDH (P605S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204091	NM_002541.4(OGDH):c.1927G>A (p.Gly643Arg)	OGDH (G639R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204092	NM_002541.4(OGDH):c.2143G>T (p.Val715Leu)	OGDH (V715L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302199	NM_002541.4(OGDH):c.2258C>T (p.Thr753Met)	OGDH (T749M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622156	NM_002541.4(OGDH):c.2374T>G (p.Ser792Ala)	OGDH (S803A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1029459	NM_002541.4(OGDH):c.2422G>A (p.Val808Ile)	OGDH (V808I +2 more)	Single nucleotide variant (missense variant)	Oxoglutaricaciduria +2 more	GUncertain significance
Select item 1492984	NM_002541.4(OGDH):c.2433C>A (p.Asp811Glu)	OGDH (D807E +2 more)	Single nucleotide variant (missense variant)	Oxoglutaricaciduria +1 more	GUncertain significance
Select item 2386849	NM_002541.4(OGDH):c.2447A>G (p.Asn816Ser)	OGDH (N816S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369467	NM_002541.4(OGDH):c.2459A>G (p.Asn820Ser)	OGDH (N816S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526244	NM_002541.4(OGDH):c.2471A>T (p.Asp824Val)	OGDH (D820V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510436	NM_002541.4(OGDH):c.2597C>G (p.Pro866Arg)	OGDH (P862R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285986	NM_002541.4(OGDH):c.2619T>G (p.Asp873Glu)	OGDH (D869E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204093	NM_002541.4(OGDH):c.2711G>C (p.Cys904Ser)	OGDH (C900S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319260	NM_002541.4(OGDH):c.2743G>A (p.Glu915Lys)	OGDH (E911K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302197	NM_002541.4(OGDH):c.2746C>T (p.Arg916Cys)	OGDH (R916C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353593	NM_002541.4(OGDH):c.3011C>T (p.Thr1004Met)	OGDH (T1000M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30