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.

6 entries on 1 page. Showing entries 1 - 6.
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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.633T>A r.(?) p.(Asp211Glu) - Parent #2 - likely pathogenic g.99008393T>A g.98391930T>A CNGA3 c.[513G>T];[633T>A] - CNGA3_000189 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 11802 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. - c.633T>A r.(?) p.(Asp211Glu) - Both (homozygous) - likely pathogenic g.99008393T>A g.98391930T>A CNGA3 c.633T>A, p.D211E - CNGA3_000189 homozygous PubMed: Liang 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease F5-II1 PubMed: Liang 2015 - M - China - - - - - 1 LOVD
+?/. - c.633T>A r.(?) p.(Asp211Glu) - Parent #1 - likely pathogenic g.99008393T>A g.98391930T>A CNGA3 c.633T>A, p.D211E - CNGA3_000189 heterozygous PubMed: Liang 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease F6-II1 PubMed: Liang 2015 - M - China - - - - - 1 LOVD
+?/. - c.633T>A r.(?) p.(Asp211Glu) - Maternal (confirmed) - likely pathogenic g.99008393T>A g.98391930T>A CNGA3 c.633T>A (p.D211E) - CNGA3_000189 - PubMed: Chen 2015 - - Germline yes - - - - DNA SEQ-NG - tagreted next-generation sequencing retinal disease Family1?II:2 PubMed: Chen 2015 - M no China - - - - - 1 LOVD
+?/. - c.633T>A r.(?) p.(Asp211Glu) TM2 Unknown - likely pathogenic (recessive) g.99008393T>A g.98391930T>A - - CNGA3_000189 ACMG PM2_mod, PP2_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.633T>A - p.Asp211Glu TM2 Unknown - NA g.99008393T>A g.98391930T>A - - CNGA3_000189 in vitro functional analysis normalized overall luminescence signal (AUC) 0.03±0.00 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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