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.

12 entries on 1 page. Showing entries 1 - 12.
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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.967G>C r.(?) p.(Ala323Pro) - Unknown - pathogenic (recessive) g.99012600G>C - 2:99012600G>C ENST00000393504.1:c.967G>C (Ala323Pro) - CNGA3_000104 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001017 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Africa - - - - 1 LOVD
+?/. - c.967G>C r.(?) p.(Ala323Pro) - Both (homozygous) - likely pathogenic g.99012600G>C g.98396137G>C c.967G>C; p.(Ala323Pro) - CNGA3_000104 - PubMed: Abdelkader 2018 - - Germline yes - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease 4 PubMed: Abdelkader 2018 - M yes - - - - - - 1 LOVD
+?/. - c.967G>C r.(?) p.(Ala323Pro) - Unknown - likely pathogenic g.99012600G>C g.98396137G>C Allele 1 c.1495C>T (p.Arg499*), Allele 2 c.967G>C (p.Ala323Pro) - CNGA3_000104 heterozygous PubMed: Khan 2019 - - Germline/De novo (untested) ? - - - - DNA ? - retrospective study retinal disease - PubMed: Khan 2019 - M - - - - - - - 1 LOVD
+?/. - c.967G>C r.(?) p.(Ala323Pro) - Unknown - likely pathogenic g.99012600G>C g.98396137G>C CNGA3 c.967G>C, p.Ala323Pro - CNGA3_000104 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001017 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.967G>C r.(?) p.(Ala323Pro) - Unknown - likely pathogenic g.99012600G>C g.98396137G>C CNGA3 c.967G>C p.(Ala323Pro) - CNGA3_000104 heterozygous PubMed: Méjécase 2020 - - Unknown ? - - - - DNA SEQ-NG - retrospective case note review, targeted gene panel testing retinal disease 56 {PMID:Méjécase 2020:3278337 - ? - United Arab Emirates - - - - - 1 LOVD
+/. - c.967G>C r.(?) p.(Ala323Pro) - Parent #1 ACMG pathogenic g.99012600G>C g.98396137G>C - - CNGA3_000104 - PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - - Germline - - - - - DNA MIPsm - smMIPs 105 iMD/AMD genes retinal disease 070668 PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - F - - - - - - - 1 Rebekkah Hitti-Malin
+?/. - c.967G>C r.(?) p.(Ala323Pro) - Parent #2 ACMG likely pathogenic g.99012600G>C g.98396137G>C CNGA3 c.967G>C - CNGA3_000104 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.967G>C r.(?) p.(Ala323Pro) - Parent #1 ACMG likely pathogenic g.99012600G>C g.98396137G>C CNGA3 c.967G>C - CNGA3_000104 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.967G>C r.(?) p.(Ala323Pro) - Parent #1 ACMG likely pathogenic g.99012600G>C g.98396137G>C CNGA3 c.967G>C - CNGA3_000104 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.967G>C r.(?) p.(Ala323Pro) - Both (homozygous) ACMG likely pathogenic g.99012600G>C g.98396137G>C CNGA3 c.967G>C - CNGA3_000104 homozygous 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.967G>C r.(?) p.(Ala323Pro) TM5 Unknown - pathogenic (recessive) g.99012600G>C g.98396137G>C - - CNGA3_000104 ACMG PS4_mod, PP5_mod, PM1_mod, PP2_sup, PM2_mod, PM5_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.967G>C - p.Ala323Pro TM5 Unknown - NA g.99012600G>C g.98396137G>C - - CNGA3_000104 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.00 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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