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.1687C > T r.(?) p.(Arg563Cys) - Parent #2 - likely pathogenic g.99013320C>T g.98396857C>T CNGA3 allele 1/allele 2: R277C/R563C - CNGA3_000183 no cDNA annotation given, variant extrapolated from literature PubMed: Koeppen 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO463 PubMed: Koeppen 2008 - M - - - - - - - 1 LOVD
+?/. 8 c.1687C>T r.(?) p.(Arg563Cys) - Unknown - likely pathogenic g.99013320C>T - c.1687C>T - CNGA3_000183 - PubMed: Maggi_2021 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Maggi_2021 - M - Switzerland - - - - - 1 LOVD
+?/. - c.1687C>T r.(?) p.(Arg563Cys) - Parent #2 - likely pathogenic g.99013320C>T g.98396857C>T CNGA3 c.[1306C>T];[1687C>T] - CNGA3_000183 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 17281 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. p.(Arg563Cys) c.1687C>T r.(?) p.(Arg563Cys) - Parent #1 - likely pathogenic g.99013320C>T g.98396857C>T CNGA3 1687C>T, Arg563Cys - CNGA3_000183 heterozygous PubMed: Georgiou 2019 - - Unknown ? - - - - DNA ? - retrospective research retinal disease JC_0578 PubMed: Georgiou 2019 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.1687C>T r.(?) p.(Arg563Cys) - Parent #2 ACMG pathogenic g.99013320C>T g.98396857C>T CNGA3 c.1687C>T - CNGA3_000183 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.1687C>T r.(?) p.(Arg563Cys) - Parent #2 ACMG pathogenic g.99013320C>T g.98396857C>T CNGA3 c.1687C>T - CNGA3_000183 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
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