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.

9 entries on 1 page. Showing entries 1 - 9.
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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.1981C>A r.(?) p.(Arg661Ser) - Parent #2 - likely pathogenic g.99013614C>A g.98397151C>A CNGA3 c.847C>T; c.1981C>A - CNGA3_000173 no protein change given, compound heterozygous PubMed: Zanolli 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 24 PubMed: Zanolli 2020 individual ID not present in paper, consecutive numbers given ? - Chile - - - - - 1 LOVD
+?/. - c.1981C>A r.(?) p.(Arg661Ser) - Parent #2 - likely pathogenic g.99013614C>A g.98397151C>A CNGA3 c.847C>T; c.1981C>A - CNGA3_000173 no protein change given, compound heterozygous PubMed: Zanolli 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 25 PubMed: Zanolli 2020 individual ID not present in paper, consecutive numbers given ? - Chile - - - - - 1 LOVD
+?/. - c.1981C>A r.(?) p.(Arg661Ser) - Parent #2 - likely pathogenic g.99013614C>A g.98397151C>A CNGA3 heterozygous c.940-942delATC, p.R661S:c.1981C>A - CNGA3_000173 - PubMed: Yang 2014 - - Unknown ? - - - - DNA SEQ blood - retinal disease 2 PubMed: Yang 2014 - F - - - - - - - 1 LOVD
+?/. - c.1981C>A r.(?) p.(Arg661Ser) - Parent #2 - likely pathogenic g.99013614C>A g.98397151C>A c.1114C>T I c.1981C>A - CNGA3_000173 heterozygous PubMed: Zelinger 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD2786 PubMed: Zelinger 2015 - - no United States Spanish - - - - 1 LOVD
+?/. - c.1981C>A r.(1981c>a) p.(Arg661Ser) - Unknown ACMG likely pathogenic g.99013614C>A - - - CNGA3_000173 - - - - De novo - - - - - DNA CMC - - maculopathy - - - - - Mexico - - - - - 1 Oscar F Chacon-Camacho
+?/. - c.1981C>A r.(?) p.(Arg661Ser) - Parent #2 ACMG likely pathogenic g.99013614C>A g.98397151C>A CNGA3 c.1981C>A - CNGA3_000173 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.1981C>A r.(?) p.(Arg661Ser) - Parent #2 ACMG likely pathogenic g.99013614C>A g.98397151C>A CNGA3 c.1981C>A - CNGA3_000173 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 2; segregation analysis: both parents: 2, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.1981C>A r.(?) p.(Arg661Ser) CLZ Unknown - pathogenic (recessive) g.99013614C>A g.98397151C>A - - CNGA3_000173 ACMG PP1_sup, PP5_strong, PM2_mod, PP3_sup, PP2_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1981C>A - p.Arg661Ser CLZ Unknown - NA g.99013614C>A g.98397151C>A - - CNGA3_000173 in vitro functional analysis normalized overall luminescence signal (AUC) 0.79±0.08, normalized peak latency 0.53±0.03 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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