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.

7 entries on 1 page. Showing entries 1 - 7.
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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.989T>C r.(?) p.(Phe330Ser) - Parent #1 - likely pathogenic (recessive) g.99012622T>C g.98396159T>C - - CNGA3_000127 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT128 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.989T>C r.(?) p.(Phe330Ser) - Parent #1 - likely pathogenic (recessive) g.99012622T>C g.98396159T>C - - CNGA3_000127 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT549 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.989T>C r.(?) p.(Phe330Ser) - Both (homozygous) - likely pathogenic g.99012622T>C g.98396159T>C c.989T>C, p.(Phe330Ser) - CNGA3_000127 Homozygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 10906 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.989T>C r.(?) p.(Phe330Ser) - Unknown - likely pathogenic g.99012622T>C g.98396159T>C c.989T>C, p.(Phe330Ser) - CNGA3_000127 compound heterozygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 14476 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.989T>C r.(?) p.(Phe330Ser) - Unknown - likely pathogenic g.99012622T>C g.98396159T>C c.989T>C, p.(Phe330Ser) - CNGA3_000127 compound heterozygous PubMed: Wang 2019 - - Germline yes - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 14652 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+/. - c.989T>C r.(?) p.(Phe330Ser) TM5 - pore helix Unknown - pathogenic (recessive) g.99012622T>C g.98396159T>C - - CNGA3_000127 ACMG PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.989T>C - p.Phe330Ser TM5 - pore helix Unknown - NA g.99012622T>C g.98396159T>C - - CNGA3_000127 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.00 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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