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.

11 entries on 1 page. Showing entries 1 - 11.
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.822G>T r.(?) p.(Arg274Ser) - Unknown - pathogenic g.99012455G>T g.98395992G>T CNGA3(NM_001298.3):c.822G>T (p.R274S) - CNGA3_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.822G>T r.(?) p.(Arg274Ser) - Unknown - pathogenic g.99012455G>T g.98395992G>T CNGA3(NM_001298.3):c.822G>T (p.R274S) - CNGA3_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 8 c.822G>T r.(?) p.(Arg274Ser) - Both (homozygous) - pathogenic g.99012455G>T - c.822G>T - CNGA3_000032 - PubMed: Azam 2010 - - Germline - - - - - DNA arraySNP, PCR blood - retinal disease - PubMed: Azam 2010 - M no Pakistan Pakistani - - - - 1 LOVD
+/. 8 c.822G>T r.(?) p.(Arg274Ser) - Both (homozygous) - pathogenic g.99012455G>T - c.822G>T - CNGA3_000032 - PubMed: Azam 2010 - - Germline - - - - - DNA arraySNP, PCR blood - retinal disease - PubMed: Azam 2010 - F no Pakistan Pakistani - - - - 1 LOVD
+/. 8 c.822G>T r.(?) p.(Arg274Ser) - Both (homozygous) - pathogenic g.99012455G>T - c.822G>T - CNGA3_000032 - PubMed: Azam 2010 - - Germline - - - - - DNA arraySNP, PCR blood - retinal disease - PubMed: Azam 2010 - M no Pakistan Pakistani - - - - 1 LOVD
+/. 8 c.822G>T r.(?) p.(Arg274Ser) - Both (homozygous) - pathogenic g.99012455G>T - c.822G>T - CNGA3_000032 - PubMed: Azam 2010 - - Germline - - - - - DNA arraySNP, PCR blood - retinal disease - PubMed: Azam 2010 - M no Pakistan Pakistani - - - - 1 LOVD
?/. 8 c.822G>T r.(?) p.(Arg274Ser) - Both (homozygous) - VUS g.99012455G>T - c.822G>T - CNGA3_000032 - PubMed: Azam-2011 - - Unknown - - - - - DNA arraySNP - - retinal disease - PubMed: Azam-2011 - - yes Pakistan pakistani - - - - 1 LOVD
+?/. - c.822G>T r.(?) p.(Arg274Ser) - Both (homozygous) ACMG likely pathogenic g.99012455G>T g.98395992G>T CNGA3 c.822G>T - CNGA3_000032 homozygous 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.822G>T r.(?) p.(Arg274Ser) - Unknown ACMG likely pathogenic (recessive) g.99012455G>T g.98395992G>T - - CNGA3_000032 ACMG PP3, PM2, PM1, PP2 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? ACHM-1272 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
+/. - c.822G>T r.(?) p.(Arg274Ser) TM4 Unknown - pathogenic (recessive) g.99012455G>T g.98395992G>T - - CNGA3_000032 ACMG PM1_mod, PP2_sup, PM2_mod, PP3_sup, PM5_mod, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.822G>T - p.Arg274Ser TM4 Unknown - NA g.99012455G>T g.98395992G>T - - CNGA3_000032 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.