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.

3 entries on 1 page. Showing entries 1 - 3.
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     
-?/. 3 c.211G>A r.211g>a p.Ala71Thr - Unknown - NA g.98994259G>A g.98377796G>A - - CNGA3_000301 analysis variant in in vitro mini-gene splicing assay PubMed: Reuter 2021 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
-?/. 3 c.211G>A r.(211g>a) p.(Ala71Thr) N-Term Unknown ACMG likely benign g.98994259G>A g.98377796G>A - - CNGA3_000301 ACMG PM2_mod, BP4_sup, BS3_strong PubMed: Solaki 2023 VCV000858875 - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.211G>A - p.Ala71Thr N-Term Unknown - NA g.98994259G>A g.98377796G>A - - CNGA3_000301 in vitro functional analysis normalized overall luminescence signal (AUC) 0.85±0.00, normalized peak latency 0.89±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  


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