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.
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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.1190G>T r.(?) p.(Gly397Val) - Unknown - likely pathogenic g.99012823G>T g.98396360G>T Allele 1 c.847C>T (pArg283Trp), Allele 2 c.1190G>T (p.Gly397Val) - CNGA3_000169 heterozygous PubMed: Khan 2019 - - Germline/De novo (untested) ? - - - - DNA ? - retrospective study retinal disease - PubMed: Khan 2019 - M - - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Parent #1 - likely pathogenic g.99012823G>T g.98396360G>T - - CNGA3_000169 homozygous PubMed: Ahuja 2008 - - Germline yes - - - - DNA DHPLC, SEQ blood index case: mutation identified with DHPLC retinal disease III:6 PubMed: Ahuja 2008 Family A, individual III:6 F yes - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Both (homozygous) - likely pathogenic g.99012823G>T g.98396360G>T - - CNGA3_000169 homozygous PubMed: Ahuja 2008 - - Germline yes - - - - DNA DHPLC, SEQ blood index case: mutation identified with DHPLC retinal disease III:7 PubMed: Ahuja 2008 Family A, individual III:7 M yes - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Both (homozygous) - likely pathogenic g.99012823G>T g.98396360G>T - - CNGA3_000169 homozygous PubMed: Ahuja 2008 - - Germline yes - - - - DNA DHPLC, SEQ blood index case: mutation identified with DHPLC retinal disease III:8 PubMed: Ahuja 2008 Family A, individual III:8 F yes - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Parent #2 - likely pathogenic g.99012823G>T g.98396360G>T - - CNGA3_000169 heterozygous PubMed: Ahuja 2008 - - Germline yes - - - - DNA DHPLC, SEQ blood index case: mutation identified with DHPLC retinal disease IV:1 PubMed: Ahuja 2008 Family A, individual IV:1 F no - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Parent #2 - likely pathogenic g.99012823G>T g.98396360G>T - - CNGA3_000169 heterozygous PubMed: Ahuja 2008 - - Germline yes - - - - DNA DHPLC, SEQ blood index case: mutation identified with DHPLC retinal disease IV:2 PubMed: Ahuja 2008 Family A, individual IV:2 M no - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Both (homozygous) ACMG likely pathogenic g.99012823G>T g.98396360G>T CNGA3 c.1190G>T - CNGA3_000169 homozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 3; segregation analysis: both parents: 0, one parent or other relatives: 3; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+?/. - c.1190G>T r.(?) p.(Gly397Val) - Parent #2 ACMG likely pathogenic g.99012823G>T g.98396360G>T CNGA3 c.1190G>T - CNGA3_000169 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - 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.1190G>T r.(?) p.(Gly397Val) - Paternal (confirmed) - likely pathogenic g.99012823G>T g.98396360G>T - - CNGA3_000169 - PubMed: Moon 2021 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel retinal disease Pat10 PubMed: Moon 2021 - - - Korea - - - - - 1 Johan den Dunnen
+/. - c.1190G>T r.(?) p.(Gly397Val) TM6 Unknown - pathogenic (recessive) g.99012823G>T g.98396360G>T - - CNGA3_000169 ACMG PP1_sup, PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1190G>T - p.Gly397Val TM6 Unknown - NA g.99012823G>T g.98396360G>T - - CNGA3_000169 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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