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.

7 entries on 1 page. Showing entries 1 - 7.
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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.1070A>G r.(?) p.(Tyr357Cys) - Parent #1 - likely pathogenic g.99012703A>G g.98396240A>G - - CNGA3_000148 - PubMed: Greenberg 2014 - - Germline - - - - - DNA SEQ - - retinal disease Pat8 PubMed: Greenberg 2014 patient - - United States - - - - - 1 LOVD
+?/. - c.1070A>G r.(?) p.(Tyr357Cys) - Parent #1 - likely pathogenic g.99012703A>G g.98396240A>G c.1070 A > G (Tyr357Cys; novel) - CNGA3_000148 heterozygous PubMed: Vincent 2011 - - Germline ? - - - - DNA SEQ blood - retinal disease 1 PubMed: Vincent 2011 - M - Canada - - - - - 1 LOVD
+?/. - c.1070A>G r.(?) p.(Tyr357Cys) - Parent #1 - likely pathogenic g.99012703A>G g.98396240A>G CNGA3 heterozygous p.Y357C:c.1070A>G, p.T565M:c.1694C>T - CNGA3_000148 - PubMed: Yang 2014 - - Unknown ? - - - - DNA SEQ blood - retinal disease 6 PubMed: Yang 2014 - F - - - - - - - 1 LOVD
+?/. - c.1070A>G r.(?) p.(Tyr357Cys) - Parent #2 ACMG likely pathogenic g.99012703A>G g.98396240A>G CNGA3 c.1070A>G - CNGA3_000148 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: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+?/. - c.1070A>G r.(?) p.(Tyr357Cys) - Parent #2 ACMG likely pathogenic g.99012703A>G g.98396240A>G CNGA3 c.1070A>G - CNGA3_000148 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.1070A>G r.(?) p.(Tyr357Cys) Pore helix Unknown - pathogenic (recessive) g.99012703A>G g.98396240A>G - - CNGA3_000148 ACMG PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1070A>G - p.Tyr357Cys Pore helix Unknown - NA g.99012703A>G g.98396240A>G - - CNGA3_000148 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.00 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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