"Ambry Genetics"[submitter] AND "OGFOD2"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457994	NM_001304833.2(OGFOD2):c.209G>A (p.Arg70Gln)	OGFOD2 (R10Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405237	NM_001304833.2(OGFOD2):c.211C>T (p.Arg71Trp)	OGFOD2 (R11W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204120	NM_001304833.2(OGFOD2):c.238G>A (p.Ala80Thr)	OGFOD2 (A80T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547426	NM_001304833.2(OGFOD2):c.272C>T (p.Pro91Leu)	OGFOD2 (P31L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591556	NM_001304833.2(OGFOD2):c.385C>T (p.Arg129Trp)	OGFOD2 (R129W +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2204948	NM_001304833.2(OGFOD2):c.406G>A (p.Glu136Lys)	OGFOD2 (E76K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350632	NM_001304833.2(OGFOD2):c.446T>C (p.Phe149Ser)	OGFOD2 (F149S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204115	NM_001304833.2(OGFOD2):c.449G>A (p.Cys150Tyr)	OGFOD2 (C150Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596324	NM_001304833.2(OGFOD2):c.490G>C (p.Asp164His)	OGFOD2 (D104H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619745	NM_001304833.2(OGFOD2):c.512A>G (p.Asn171Ser)	OGFOD2 (N7S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204116	NM_001304833.2(OGFOD2):c.550G>A (p.Gly184Arg)	OGFOD2 (G124R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215770	NM_001304833.2(OGFOD2):c.559G>A (p.Glu187Lys)	OGFOD2 (E127K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369353	NM_001304833.2(OGFOD2):c.586C>T (p.Arg196Cys)	OGFOD2 (R196C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601321	NM_001304833.2(OGFOD2):c.593T>C (p.Leu198Pro)	OGFOD2 (L198P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410833	NM_001304833.2(OGFOD2):c.643G>A (p.Asp215Asn)	OGFOD2 (D215N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546659	NM_001304833.2(OGFOD2):c.698G>A (p.Gly233Asp)	OGFOD2 (G233D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548554	NM_001304833.2(OGFOD2):c.718G>A (p.Glu240Lys)	OGFOD2 (E240K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204117	NM_001304833.2(OGFOD2):c.730A>G (p.Asn244Asp)	OGFOD2 (N80D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204118	NM_001304833.2(OGFOD2):c.731A>G (p.Asn244Ser)	OGFOD2 (N184S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527958	NM_001304833.2(OGFOD2):c.743G>C (p.Gly248Ala)	OGFOD2 (G188A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512200	NM_001304833.2(OGFOD2):c.763G>A (p.Ala255Thr)	OGFOD2 (A255T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373329	NM_001304833.2(OGFOD2):c.767T>C (p.Leu256Pro)	OGFOD2 (L256P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527806	NM_001304833.2(OGFOD2):c.859G>A (p.Gly287Ser)	OGFOD2 (G287S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463851	NM_001304833.2(OGFOD2):c.868C>T (p.His290Tyr)	OGFOD2 (H230Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204121	NM_001304833.2(OGFOD2):c.877C>T (p.Arg293Trp)	OGFOD2 (R129W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221122	NM_001304833.2(OGFOD2):c.938G>A (p.Arg313His)	OGFOD2 (R313H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204122	NM_001304833.2(OGFOD2):c.965G>A (p.Arg322His)	OGFOD2 (R262H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204123	NM_001304833.2(OGFOD2):c.973G>A (p.Asp325Asn)	OGFOD2 (D265N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204124	NM_001304833.2(OGFOD2):c.997G>A (p.Gly333Ser)	OGFOD2 (G273S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2617924	NM_001304833.2(OGFOD2):c.1010C>T (p.Thr337Ile)	OGFOD2 (T277I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204125	NM_001304833.2(OGFOD2):c.1018G>A (p.Glu340Lys)	OGFOD2 (E176K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412548	NM_001304833.2(OGFOD2):c.1028C>T (p.Thr343Met)	OGFOD2 (T179M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204126	NM_001304833.2(OGFOD2):c.1043C>T (p.Ala348Val)	OGFOD2 (A184V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33