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.1030G>T r.(?) p.(Glu344*) - Parent #2 - likely pathogenic g.99012663G>T - p.E344X - CNGA3_000097 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. 8 c.1030G>T r.(?) p.(Glu344*) - Parent #1 - likely pathogenic g.99012663G>T - p.E344X - CNGA3_000097 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+/. - c.1030G>T r.(?) p.(Glu344*) - Unknown - pathogenic g.99012663G>T g.98396200G>T CNGA3 c.1030G>T, p.Glu344Ter - CNGA3_000097 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2924_004509 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.1030G>T r.(?) p.(Glu344*) - Parent #1 ACMG likely pathogenic g.99012663G>T g.98396200G>T CNGA3 c.1030G>T - CNGA3_000097 heterozygous 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: 0, one parent or other relatives: 1; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+?/. - c.1030G>T r.(?) p.(Glu344*) - Parent #2 ACMG likely pathogenic g.99012663G>T g.98396200G>T CNGA3 c.1030G>T - CNGA3_000097 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: 2, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
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