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.

14 entries on 1 page. Showing entries 1 - 14.
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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     
+/. 7 c.1642G>A r.(?) p.(Gly548Arg) - Paternal (confirmed) - pathogenic g.99013275G>A g.98396812G>A - - CNGA3_000055 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - M no Israel Jewish-Oriental - - - - 1 Dror Sharon
+?/. - c.1642G>A r.(?) p.(Gly548Arg) - Unknown ACMG likely pathogenic g.99013275G>A - - - CNGA3_000055 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. 8 c.1642G>A r.(?) p.(Gly548Arg) - Both (homozygous) - pathogenic (recessive) g.99013275G>A - Gly548Arg/Gly548Arg - CNGA3_000055 - PubMed: Johnson 2004 - - Germline - - - - - DNA SEQ Blood - retinal disease - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - 1 Julia Lopez
+?/. - c.1642G>A r.(?) p.(Gly548Arg) - Maternal (confirmed) - likely pathogenic (recessive) g.99013275G>A g.98396812G>A - - CNGA3_000055 - PubMed: Rim 2017 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease Pat24 PubMed: Rim 2017 - M - Korea - - - - - 1 LOVD
+/. 8 c.1642G>A r.(?) p.(Gly548Arg) - Unknown - pathogenic g.99013275G>A - c.1642G>A - CNGA3_000055 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - M - - - - - - - 1 Julia Lopez
+?/. - c.1642G>A r.(?) p.(Gly548Arg) - Paternal (confirmed) - likely pathogenic g.99013275G>A g.98396812G>A c.1256C-->T, c.1642G-->A; p.Ser419Phe, p.Gly548Arg - CNGA3_000055 confirmed with Sanger sequencing; compound heterozygous PubMed: Patel 2019 - - Germline yes - - - - DNA SEQ-NG blood - ACHM2 268 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.1642G>A r.(?) p.(Gly548Arg) - Parent #2 - likely pathogenic g.99013275G>A g.98396812G>A CNGA3 c.[830G>A];[1642G>A] - CNGA3_000055 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 8405 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. - c.1642G>A r.(?) p.(Gly548Arg) - Parent #2 - likely pathogenic g.99013275G>A g.98396812G>A c.1585G>A I c.1642G>A - CNGA3_000055 heterozygous PubMed: Zelinger 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0013-2 PubMed: Zelinger 2015 - - no Israel Iraqi Jewish - - - - 1 LOVD
+?/. - c.1642G>A r.(?) p.(Gly548Arg) - Parent #2 - likely pathogenic g.99013275G>A g.98396812G>A CNGA3 c.1642G>A, p.G548R - CNGA3_000055 heterozygous PubMed: Liang 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease F3-II1 PubMed: Liang 2015 - F - China - - - - - 1 LOVD
+/. - c.1642G>A r.(?) p.(Gly548Arg) - Parent #2 ACMG pathogenic g.99013275G>A g.98396812G>A CNGA3 c.1642G>A - CNGA3_000055 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 2; segregation analysis: both parents: 0, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.1642G>A r.(?) p.(Gly548Arg) - Parent #2 ACMG pathogenic g.99013275G>A g.98396812G>A CNGA3 c.1642G>A - CNGA3_000055 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.1642G>A r.(?) p.(Gly548Arg) - Both (homozygous) ACMG pathogenic g.99013275G>A g.98396812G>A CNGA3 c.1642G>A - CNGA3_000055 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.1642G>A r.(?) p.(Gly548Arg) CNBD β6 Unknown - pathogenic (recessive) g.99013275G>A g.98396812G>A - - CNGA3_000055 ACMG PP1_sup, PP5_strong, PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1642G>A - p.Gly548Arg CNBD β6 Unknown - NA g.99013275G>A g.98396812G>A - - CNGA3_000055 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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