"Ambry Genetics"[submitter] AND "ODC1"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302171	NM_002539.3(ODC1):c.1345C>T (p.Arg449Cys)	ODC1 (R449C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3302172	NM_002539.3(ODC1):c.1241+2T>G	ODC1	Single nucleotide variant (splice donor variant)	Inborn genetic diseases	GUncertain significance
Select item 3204031	NM_002539.3(ODC1):c.1238C>T (p.Ala413Val)	ODC1 (A284V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2259140	NM_002539.3(ODC1):c.1125G>A (p.Met375Ile)	ODC1 (M246I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399831	NM_002539.3(ODC1):c.1036C>G (p.Pro346Ala)	ODC1 (P217A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2650673	NM_002539.3(ODC1):c.773C>T (p.Ala258Val)	ODC1 (A129V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2359088	NM_002539.3(ODC1):c.757G>C (p.Gly253Arg)	ODC1 (G253R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3204034	NM_002539.3(ODC1):c.718G>A (p.Gly240Arg)	ODC1 (G240R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343197	NM_002539.3(ODC1):c.610G>A (p.Asp204Asn)	ODC1 (D204N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3302173	NM_002539.3(ODC1):c.566T>C (p.Ile189Thr)	ODC1 (I189T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3204033	NM_002539.3(ODC1):c.533G>A (p.Arg178Lys)	ODC1 (R178K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2320097	NM_002539.3(ODC1):c.493C>T (p.Arg165Cys)	ODC1 (R165C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2389236	NM_002539.3(ODC1):c.364T>A (p.Tyr122Asn)	ODC1 (Y122N)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3204032	NM_002539.3(ODC1):c.273C>G (p.Ser91Arg)	ODC1 (S91R)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2302664	NM_002539.3(ODC1):c.247A>G (p.Thr83Ala)	ODC1 (T83A)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2529517	NM_002539.3(ODC1):c.121T>A (p.Tyr41Asn)	ODC1 (Y41N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3204035	NM_002539.3(ODC1):c.98C>T (p.Ser33Phe)	ODC1 (S33F)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2488057	NM_002539.3(ODC1):c.38T>A (p.Phe13Tyr)	ODC1 (F13Y)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance