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.

9 entries on 1 page. Showing entries 1 - 9.
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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.1405G>A r.(?) p.(Ala469Thr) - Unknown - pathogenic (recessive) g.99013038G>A - 2:99013038G>A ENST00000393504.1:c.1405G>A (Ala469Thr) - CNGA3_000105 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001017 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Africa - - - - 1 LOVD
+?/. - c.1405G>A r.(?) p.(Ala469Thr) - Unknown - likely pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A, p.Ala469Thr - CNGA3_000105 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001017 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.1405G>A r.(?) p.(Ala469Thr) - Maternal (confirmed) ACMG likely pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A, p.(Ala469Thr) - CNGA3_000105 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-432 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband M - Spain - - - - - 1 LOVD
+?/. - c.1405G>A r.(?) p.(Ala469Thr) - Maternal (confirmed) ACMG likely pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A, p.(Ala469Thr) - CNGA3_000105 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-433 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband's sister F - Spain - - - - - 1 LOVD
+?/. - c.1405G>A r.(?) p.(Ala469Thr) - Maternal (confirmed) ACMG likely pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A, p.(Ala469Thr) - CNGA3_000105 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-432 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband M - Spain - - - - - 1 LOVD
+?/. - c.1405G>A r.(?) p.(Ala469Thr) - Maternal (confirmed) ACMG likely pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A, p.(Ala469Thr) - CNGA3_000105 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-433 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband's sister F - Spain - - - - - 1 LOVD
+?/. - c.1405G>A r.(?) p.(Ala469Thr) - Parent #1 - likely pathogenic g.99013038G>A g.98396575G>A allele 1/2: A469T/R277C - CNGA3_000105 heterozygous PubMed: Reuter 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO439 PubMed: Reuter 2008 - F - Germany - - - - - 1 LOVD
+/. - c.1405G>A r.(?) p.(Ala469Thr) - Parent #2 ACMG pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A - CNGA3_000105 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.1405G>A r.(?) p.(Ala469Thr) - Parent #2 ACMG pathogenic g.99013038G>A g.98396575G>A CNGA3 c.1405G>A - CNGA3_000105 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 2 ; number of affected individuals: 3; segregation analysis: both parents: 0, one parent or other relatives: 2; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
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