"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ODAD1"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 241875	NM_001364171.2(ODAD1):c.1788C>T (p.His596=)	ODAD1	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 39640	NM_001364171.2(ODAD1):c.1502+5G>A	ODAD1	Single nucleotide variant (intron variant)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 262488	NM_001364171.2(ODAD1):c.1481C>T (p.Pro494Leu)	ODAD1 (P457L +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 691976	NM_001364171.2(ODAD1):c.1336C>T (p.Leu446Phe)	ODAD1 (L409F +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1129994	NM_001364171.2(ODAD1):c.1272C>T (p.Cys424=)	ODAD1	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia +1 more	GLikely benign
Select item 39637	NM_001364171.2(ODAD1):c.853G>A (p.Ala285Thr)	ODAD1 (A248T +1 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 20 +2 more	GPathogenic
Select item 39639	NM_001364171.2(ODAD1):c.598-2A>G	ODAD1	Single nucleotide variant (splice acceptor variant)	not provided +1 more	GPathogenic
Select item 262499	NM_001364171.2(ODAD1):c.582C>T (p.Asp194=)	ODAD1	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 454971	NM_001364171.2(ODAD1):c.522G>A (p.Ala174=)	ODAD1	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia +1 more	GBenign/Likely benign
Select item 696643	NM_001364171.2(ODAD1):c.414G>A (p.Pro138=)	ODAD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign