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     
?/. 6 c.556C>T r.(?) p.(Leu186Phe) - Parent #1 - pathogenic (recessive) g.99006227C>T - 556C>T(L186F) - CNGA3_000088 - PubMed: Eksandh 2002 - - Germline ? - - - - DNA SEQ - - retinal disease FamBPatII1 PubMed: Eksandh 2002 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Sweden - - - - - 1 Julia Lopez
+?/. - c.556C>T r.(?) p.(Leu186Phe) - Unknown - likely pathogenic g.99006227C>T g.98389764C>T - - CNGA3_000088 - PubMed: Patel 2016 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease 13DG0540 PubMed: Patel 2016 - - - Saudi Arabia - - - - - 1 LOVD
+?/. - c.556C>T r.(?) p.(Leu186Phe) - Both (homozygous) ACMG likely pathogenic (recessive) g.99006227C>T g.98389764C>T NM_001298.2:c.556C>T;p.(Leu186Phe) - CNGA3_000088 - PubMed: Patel 2018 - - Germline yes - - - - DNA SEQ-NG - 322 eye disease gene panel retinal disease 11DG0997 PubMed: Patel 2018 - - likely Saudi Arabia - - - - - 1 LOVD
+?/. 5 c.556C>T r.(?) p.(Leu186Phe) - Parent #1 - likely pathogenic g.99006227C>T g.98389764C>T allele 1/2: L186F/R277C - CNGA3_000088 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO47/C PubMed: Wissinger 2001 - F - Sweden - - - - - 1 LOVD
+?/. - c.556C>T r.(?) p.(Leu186Phe) - Parent #2 ACMG likely pathogenic g.99006227C>T g.98389764C>T CNGA3 c.556C>T - CNGA3_000088 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
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