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     
+?/. 8 c.1201T>C r.(?) p.(Ser401Pro) - Parent #1 - likely pathogenic (recessive) g.99012834T>C - p.S401P - CNGA3_000098 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. 8 c.1201T>C r.(?) p.(Ser401Pro) - Both (homozygous) - likely pathogenic g.99012834T>C - p.S401P - CNGA3_000098 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. - c.1201T>C r.(?) p.(Ser401Pro) - Parent #2 ACMG likely pathogenic g.99012834T>C g.98396371T>C CNGA3 c.1201T>C - CNGA3_000098 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 1; segregation analysis: both parents: 0, one parent or other relatives: 0; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
+?/. - c.1201T>C r.(?) p.(Ser401Pro) - Parent #2 ACMG likely pathogenic g.99012834T>C g.98396371T>C CNGA3 c.1201T>C - CNGA3_000098 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 1; segregation analysis: both parents: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.1201T>C r.(?) p.(Ser401Pro) TM6 Unknown - pathogenic (recessive) g.99012834T>C g.98396371T>C - - CNGA3_000098 ACMG PP1_sup, PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1201T>C - p.Ser401Pro TM6 Unknown - NA g.99012834T>C g.98396371T>C - - CNGA3_000098 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±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.