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.
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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.1243G>C r.(?) p.(Ala415Pro) - Parent #2 - likely pathogenic g.99012876G>C g.98396413G>C - - CNGA3_000111 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 456 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+/. - c.1243G>C r.(?) p.(Ala415Pro) C-linker αA Unknown - pathogenic (recessive) g.99012876G>C g.98396413G>C - - CNGA3_000111 ACMG PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1243G>C - p.Ala415Pro C-linker αA Unknown - NA g.99012876G>C g.98396413G>C - - CNGA3_000111 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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