Full data view for gene CNGA3

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_001298.2 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.512G>A r.(?) p.(Trp171Ter) - Both (homozygous) - likely pathogenic (recessive) g.99006183G>A g.98389720G>A - - CNGA3_000117 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT144 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.512G>A r.(?) p.(Trp171Ter) - Parent #1 - likely pathogenic (recessive) g.99006183G>A g.98389720G>A - - CNGA3_000117 - PubMed: Huang 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease QT1270 PubMed: Huang 2016 - - - China - - - - - 1 Johan den Dunnen
+?/. - c.512G>A r.(?) p.(Trp171*) - Both (homozygous) - likely pathogenic g.99006183G>A g.98389720G>A c.512G>A, p.(Trp153*) - CNGA3_000117 different transcript anderror in annotation: NM_001079878.1(CNGA3)c.458G>A causes p.(Trp153*), Homozygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 11069 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.512G>A r.(?) p.(Trp171*) - Unknown - likely pathogenic g.99006183G>A g.98389720G>A c.512G>A, p.(Trp171*) - CNGA3_000117 compound heterozygous PubMed: Wang 2019 - - Germline yes - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13150 PubMed: Wang 2019 - F - China - - - - - 1 LOVD
+/. - c.512G>A r.(?) p.(Trp171*) - Unknown - pathogenic g.99006183G>A g.98389720G>A c.512G>A, p.(Trp171*) - CNGA3_000117 single heterozygous variant in a recessive gene PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 6683 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.512G>A r.(?) p.(Trp171*) - Parent #1 - likely pathogenic g.99006183G>A g.98389720G>A CNGA3 c.[512G>A];[1585G>A] - CNGA3_000117 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 11787 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.