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.1705C>T r.(?) p.(Arg569Cys) - Unknown - VUS g.99013338C>T g.98396875C>T CNGA3(NM_001298.3):c.1705C>T (p.R569C) - CNGA3_000073 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1705C>T r.(?) p.(Arg569Cys) - Unknown - likely pathogenic g.99013338C>T g.98396875C>T CNGA3 c.170SC >T p.(Arg569Cys) - CNGA3_000073 heterozygous PubMed: Méjécase 2020 - - Unknown ? - - - - DNA SEQ-NG - retrospective case note review, targeted gene panel testing retinal disease 56 {PMID:Méjécase 2020:3278337 - ? - United Arab Emirates - - - - - 1 LOVD
+?/. - c.1705C>T r.(?) p.(Arg569Cys) - Parent #1 ACMG likely pathogenic g.99013338C>T g.98396875C>T CNGA3 c.1705C>T - CNGA3_000073 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.1705C>T r.(?) p.(Arg569Cys) CNBD β7 Unknown - pathogenic (recessive) g.99013338C>T g.98396875C>T - - CNGA3_000073 ACMG PM1_mod, PP2_sup, PM2_mod, PM5_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1705C>T - p.Arg569Cys CNBD β7 Unknown - NA g.99013338C>T g.98396875C>T - - CNGA3_000073 in vitro functional analysis normalized overall luminescence signal (AUC) 0.29±0.05, normalized peak latency 1.85±0.04 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1705C>T r.(?) p.(Arg569Cys) - Parent #2 - likely pathogenic g.99013338C>T g.98396875C>T - - CNGA3_000073 - PubMed: Midgley 2024 - rs757167624 Germline - - - - - DNA SEQ-NG - gene panel retinal disease Pat66 PubMed: Midgley 2024 - F - South Africa Africa-indigenous - - - - 1 Johan den Dunnen
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