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.

3 entries on 1 page. Showing entries 1 - 3.
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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.796G>A r.(?) p.(Val266Met) - Unknown - likely pathogenic g.99012429G>A - c.796G>A (p.V266M) - CNGA3_000152 - PubMed: Thiadens_2010 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Thiadens_2010 - M - Netherlands - - - - - 1 LOVD
-?/. - c.796G>A r.(?) p.(Val266Met) TM3 - TM4 Unknown - likely benign g.99012429G>A g.98395966G>A - - CNGA3_000152 ACMG PM1_mod, PP2_sup, PM2_mod, BP4_sup, BS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.796G>A - p.Val266Met TM3 - TM4 Unknown - NA g.99012429G>A g.98395966G>A - - CNGA3_000152 in vitro functional analysis normalized overall luminescence signal (AUC) 0.88±0.11, normalized peak latency 0.94±0.02 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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