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.1579C>A r.(?) p.(Leu527Met) - Both (homozygous) - pathogenic g.99013212C>A g.98396749C>A - - CNGA3_000002 not in 400 control chromosomes PubMed: Wang 2011, Journal: Wang 2011 - - Germline yes - - - - DNA SEQ, SEQ-NG - - LCA - PubMed: Wang 2011, Journal: Wang 2011 4-generation family, 1 affected, unaffected heterozygous carrier parents/sibs F yes Saudi Arabia - - - - - 1 Johan den Dunnen
+?/. - c.1579C>A r.(?) p.(Leu527Met) - Parent #2 ACMG likely pathogenic g.99013212C>A g.98396749C>A CNGA3 c.1579C>A - CNGA3_000002 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: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+?/. - c.1579C>A r.(?) p.(Leu527Met) - Parent #2 ACMG likely pathogenic g.99013212C>A g.98396749C>A CNGA3 c.1579C>A - CNGA3_000002 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
+/. - c.1579C>A r.(?) p.(Leu527Met) CNBD β4 Unknown - pathogenic (recessive) g.99013212C>A g.98396749C>A - - CNGA3_000002 ACMG PM1_mod, PP2_sup, PM2_mod, PM5_mod, PP3_sup, PP5_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1579C>A - p.Leu527Met CNBD β4 Unknown - NA g.99013212C>A g.98396749C>A - - CNGA3_000002 in vitro functional analysis normalized overall luminescence signal (AUC) 0.04±0.01, normalized peak latency 1.31±0.08 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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