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.1319G>C r.(?) p.(Trp440Ser) - Parent #1 - likely pathogenic g.99012952G>C g.98396489G>C CNGA3, variant 1: c.906G>T/p.R302S, variant 2: c.1319G>C/p.W440S - CNGA3_000181 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 1028 PubMed: Weisschuh 2020 Filing key number: 563, cone dystrophy, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. p.(Trp440Ser) c.1319G>C r.(?) p.(Trp440Ser) - Parent #2 - likely pathogenic g.99012952G>C g.98396489G>C CNGA3 1319G>C, Trp440Ser - CNGA3_000181 heterozygous PubMed: Georgiou 2019 - - Unknown ? - - - - DNA ? - retrospective research retinal disease JC_10551 PubMed: Georgiou 2019 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.1319G>C r.(?) p.(Trp440Ser) - Parent #2 ACMG likely pathogenic g.99012952G>C g.98396489G>C CNGA3 c.1319G>C - CNGA3_000181 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.1319G>C r.(?) p.(Trp440Ser) - Parent #2 ACMG likely pathogenic g.99012952G>C g.98396489G>C CNGA3 c.1319G>C - CNGA3_000181 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 1; segregation analysis: both parents: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.1319G>C r.(?) p.(Trp440Ser) C-linker αB Unknown - pathogenic (recessive) g.99012952G>C g.98396489G>C - - CNGA3_000181 ACMG PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1319G>C - p.Trp440Ser C-linker αB Unknown - NA g.99012952G>C g.98396489G>C - - CNGA3_000181 in vitro functional analysis normalized overall luminescence signal (AUC) 0.03±0.01, normalized peak latency 1.38±0.12 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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