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.

5 entries on 1 page. Showing entries 1 - 5.
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.1320G>A r.(?) p.(Trp440*) - Unknown - pathogenic g.99012953G>A g.98396490G>A CNGB3: c.[1148delC];[1578+1G>A], p.[R403Q];[?] Splice defect, CNGA3: c.[1320G>A];[=] - CNGA3_000164 - PubMed: Burkhard 2018 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - retinal disease 14 PubMed: Burkhard 2018 - F no - - - - - - 1 LOVD
+?/. 7 c.1320G>A r.(?) p.(Trp440*) - Parent #1 - likely pathogenic g.99012953G>A g.98396490G>A allele 1/2: W440X/G516E - CNGA3_000164 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO103/Km PubMed: Wissinger 2001 - M - Turkey - - - - - 1 LOVD
+?/. 7 c.1320G>A r.(?) p.(Trp440*) - Parent #1 - likely pathogenic g.99012953G>A g.98396490G>A allele 1/2: W440X/G516E - CNGA3_000164 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO103/Kz PubMed: Wissinger 2001 - F - Turkey - - - - - 1 LOVD
+?/. 7 c.1320G>A r.(?) p.(Trp440*) - Parent #1 - likely pathogenic g.99012953G>A g.98396490G>A allele 1/2: W440X/G516E - CNGA3_000164 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO103/S PubMed: Wissinger 2001 - M - Turkey - - - - - 1 LOVD
+?/. - c.1320G>A r.(?) p.(Trp440*) - Parent #1 ACMG likely pathogenic g.99012953G>A g.98396490G>A CNGA3 c.1320G>A - CNGA3_000164 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 3; segregation analysis: both parents: 3, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.