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.

8 entries on 1 page. Showing entries 1 - 8.
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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.1126G>A r.(?) p.(Glu376Lys) - Unknown - likely pathogenic g.99012759G>A - c.1126G>A - CNGA3_000179 - PubMed: Maggi_2021 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Maggi_2021 - M - Switzerland - - - - - 1 LOVD
+/. - c.1126G>A r.(?) p.(Glu376Lys) - Both (homozygous) - pathogenic g.99012759G>A g.98396296G>A CNGA3 allele 1/allele 2: E376K/E376K - CNGA3_000179 homozygous PubMed: Koeppen 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO383-12408 PubMed: Koeppen 2010 - M - Germany - - - - - 1 LOVD
+?/. - c.1126G>A r.(?) p.(Glu376Lys) - Both (homozygous) - likely pathogenic g.99012759G>A g.98396296G>A c.1126G>A I c.1126G>A - CNGA3_000179 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD4196tt PubMed: Zelinger 2015 - - no United States Old Order Amish - - - - 1 LOVD
+?/. - c.1126G>A r.(?) p.(Glu376Lys) - Both (homozygous) - likely pathogenic g.99012759G>A g.98396296G>A c.1126G>A I c.1126G>A - CNGA3_000179 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD4312tt PubMed: Zelinger 2015 - - yes United States Old Order Amish - - - - 1 LOVD
+?/. - c.1126G>A r.(?) p.(Glu376Lys) - Both (homozygous) - likely pathogenic g.99012759G>A g.98396296G>A c.1126G>A I c.1126G>A - CNGA3_000179 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD4313tt PubMed: Zelinger 2015 - - yes United States Old Order Amish - - - - 1 LOVD
+?/. - c.1126G>A r.(?) p.(Glu376Lys) - Both (homozygous) - likely pathogenic g.99012759G>A g.98396296G>A c.1126G>A I c.1126G>A - CNGA3_000179 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD3790tt PubMed: Zelinger 2015 - - no United States Old Order Amish - - - - 1 LOVD
+/. - c.1126G>A r.(?) p.(Glu376Lys) - Both (homozygous) ACMG pathogenic g.99012759G>A g.98396296G>A CNGA3 c.1126G>A - CNGA3_000179 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: 2, one parent or other relatives: 1; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.1126G>A r.(?) p.(Glu376Lys) - Parent #2 ACMG pathogenic g.99012759G>A g.98396296G>A CNGA3 c.1126G>A - CNGA3_000179 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
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