"PreventionGenetics, part of Exact Sciences"[submitter] AND "ODAD2"[ge - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 417175	NM_018076.5(ODAD2):c.3086C>T (p.Ser1029Phe)	LOC132089773, ODAD2 (S1029F +2 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 3059071	NM_018076.5(ODAD2):c.3021+7232TTAT[8]	ODAD2	Microsatellite (intron variant)	ODAD2-related disorder	GBenign
Select item 3056408	NM_018076.5(ODAD2):c.3021+7232TTAT[11]	ODAD2	Microsatellite (intron variant)	ODAD2-related disorder	GBenign
Select item 3039546	NM_018076.5(ODAD2):c.3021+7232TTAT[10]	ODAD2	Microsatellite (intron variant)	ODAD2-related disorder	GBenign
Select item 696184	NM_018076.5(ODAD2):c.2983G>A (p.Asp995Asn)	ODAD2 (D995N +2 more)	Single nucleotide variant (missense variant)	ODAD2-related disorder +3 more	GBenign/Likely benign
Select item 1100277	NM_018076.5(ODAD2):c.2592A>G (p.Pro864=)	ODAD2	Single nucleotide variant (synonymous variant)	ODAD2-related disorder +1 more	GLikely benign
Select item 221004	NM_018076.5(ODAD2):c.2342G>T (p.Gly781Val)	ODAD2 (G781V +2 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 23 +3 more	GConflicting classifications of pathogenicity
Select item 541493	NM_018076.5(ODAD2):c.2258G>A (p.Arg753Gln)	ODAD2 (R753Q +2 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +2 more	GUncertain significance
Select item 417173	NM_018076.5(ODAD2):c.2127C>T (p.Leu709=)	ODAD2	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia +2 more	GBenign/Likely benign
Select item 260994	NM_018076.5(ODAD2):c.2058T>C (p.Asn686=)	ODAD2	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia 23 +3 more	GBenign
Select item 698302	NM_018076.5(ODAD2):c.1997G>C (p.Arg666Pro)	ODAD2 (R666P +2 more)	Single nucleotide variant (missense variant)	ODAD2-related disorder +2 more	GBenign/Likely benign
Select item 1681370	NM_018076.5(ODAD2):c.1730G>T (p.Gly577Val)	ODAD2 (G102V +2 more)	Single nucleotide variant (missense variant)	ODAD2-related disorder +1 more	GUncertain significance
Select item 969626	NM_018076.5(ODAD2):c.1386+5G>A	ODAD2	Single nucleotide variant (intron variant)	Primary ciliary dyskinesia 23 +2 more	GConflicting classifications of pathogenicity
Select item 412249	NM_018076.5(ODAD2):c.1228C>G (p.Gln410Glu)	ODAD2 (Q410E +1 more)	Single nucleotide variant (missense variant +1 more)	Primary ciliary dyskinesia +2 more	GLikely benign
Select item 3048574	NM_018076.5(ODAD2):c.1173C>T (p.Asp391=)	ODAD2	Single nucleotide variant (synonymous variant +1 more)	ODAD2-related disorder	GLikely benign
Select item 3051094	NM_018076.5(ODAD2):c.1143-5dup	ODAD2	Duplication (intron variant)	ODAD2-related disorder	GLikely benign
Select item 3058580	NM_018076.5(ODAD2):c.939A>G (p.Gly313=)	ODAD2	Single nucleotide variant (synonymous variant +1 more)	ODAD2-related disorder	GLikely benign
Select item 3058289	NM_018076.5(ODAD2):c.937-8A>C	ODAD2	Single nucleotide variant (intron variant)	ODAD2-related disorder	GLikely benign
Select item 241266	NM_018076.5(ODAD2):c.883G>C (p.Val295Leu)	ODAD2 (V295L)	Single nucleotide variant (missense variant +1 more)	Primary ciliary dyskinesia +3 more	GConflicting classifications of pathogenicity
Select item 3050626	NM_018076.5(ODAD2):c.820-8dup	ODAD2	Duplication (intron variant)	ODAD2-related disorder	GLikely benign
Select item 659262	NM_018076.5(ODAD2):c.724C>T (p.Gln242Ter)	ODAD2 (Q242*)	Single nucleotide variant (nonsense)	ODAD2-related disorder +1 more	GPathogenic/Likely pathogenic
Select item 412242	NM_018076.5(ODAD2):c.583A>T (p.Ser195Cys)	ODAD2 (S195C)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 23 +2 more	GLikely benign
Select item 474588	NM_018076.5(ODAD2):c.423T>C (p.Tyr141=)	ODAD2	Single nucleotide variant (synonymous variant)	ODAD2-related disorder +2 more	GBenign/Likely benign
Select item 417170	NM_018076.5(ODAD2):c.198A>C (p.Ser66=)	LOC126860891, ODAD2	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia +2 more	GBenign/Likely benign

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Items: 24