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.
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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     
+/. 8 c.952G>A r.(?) p.(Ala318Thr) - Both (homozygous) - pathogenic g.99012585G>A g.98396122G>A - - CNGA3_000004 - PubMed: Li 2017 - - Germline yes - - - - DNA SEQ WBC - RD 61086 PubMed: Li 2017 - M yes Pakistan Pakistani - - - - 1 James Hejtmancik
+?/. - c.952G>A r.(?) p.(Ala318Thr) - Parent #1 - likely pathogenic g.99012585G>A g.98396122G>A CNGA3 c.[952G>A]; [1706G>A] - CNGA3_000004 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 5384 PubMed: Sun 2020 early childhood onset defined as younger than 8y M - China - - - - - 1 LOVD
+/. - c.952G>A r.(?) p.(Ala318Thr) - Parent #1 ACMG pathogenic g.99012585G>A g.98396122G>A CNGA3 c.952G>A - CNGA3_000004 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.952G>A r.(?) p.(Ala318Thr) TM5 Unknown - pathogenic (recessive) g.99012585G>A g.98396122G>A - - CNGA3_000004 ACMG PP1_sup, PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.952G>A - p.Ala318Thr TM5 Unknown - NA g.99012585G>A g.98396122G>A - - CNGA3_000004 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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