CDO1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2379066	NM_001801.3(CDO1):c.524A>G (p.Asn175Ser)	CDO1 (N175S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343884	NM_001801.3(CDO1):c.466T>A (p.Leu156Met)	CDO1 (L155M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516178	NM_001801.3(CDO1):c.328C>G (p.Pro110Ala)	CDO1 (P110A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3037994	NM_001801.3(CDO1):c.171-3dup	CDO1	Duplication (intron variant)	CDO1-related disorder	GLikely benign
Select item 2372833	NM_001801.3(CDO1):c.167A>G (p.Tyr56Cys)	CDO1 (Y56C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2372565	NM_001801.3(CDO1):c.151G>T (p.Ala51Ser)	CDO1 (A51S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2321213	NM_001801.3(CDO1):c.89T>C (p.Val30Ala)	CDO1 (V30A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2486827	NM_001801.3(CDO1):c.85A>G (p.Asn29Asp)	CDO1 (N29D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3141676	NM_001801.3(CDO1):c.46A>G (p.Ile16Val)	CDO1 (I16V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3141675	NM_001801.3(CDO1):c.24G>T (p.Lys8Asn)	CDO1 (K8N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance