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.

10 entries on 1 page. Showing entries 1 - 10.
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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.668G>A r.(?) p.(Arg223Gln) - Parent #1 - likely pathogenic (recessive) g.99008428G>A g.98391965G>A - - CNGA3_000118 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT389 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+/. - c.668G>A r.(?) p.(Arg223Gln) - Parent #2 - pathogenic (recessive) g.99008428G>A - - - CNGA3_000118 - PubMed: Duncker 2015 - - Germline - - - - - DNA SEQ - - retinal disease Pat24 PubMed: Duncker 2015 - M - United States black - - - - 1 Johan den Dunnen
+?/. - c.668G>A r.(?) p.(Arg223Gln) - Parent #1 - likely pathogenic g.99008428G>A g.98391965G>A - - CNGA3_000118 - PubMed: Greenberg 2014 - - Germline - - - - - DNA SEQ - - retinal disease Fam4Pat16 PubMed: Greenberg 2014 family, 2 affected - - United States - - - - - 2 LOVD
+?/. - c.668G>A r.(?) p.(Arg223Gln) - Parent #1 - likely pathogenic g.99008428G>A g.98391965G>A - - CNGA3_000118 - PubMed: Greenberg 2014 - - Germline - - - - - DNA SEQ - - retinal disease Fam4Pat17 PubMed: Greenberg 2014 sib - - United States - - - - - 1 LOVD
+?/. - c.668G>A r.(?) p.(Arg223Gln) - Parent #1 - likely pathogenic g.99008428G>A g.98391965G>A CNGA3, variant 1: c.668G>A/p.R223Q, variant 2: c.1306C>T/p.R436W - CNGA3_000118 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 1281 PubMed: Weisschuh 2020 Filing key number: 1105, achromatopsia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.668G>A r.(?) p.(Arg223Gln) - Parent #2 ACMG pathogenic g.99008428G>A g.98391965G>A CNGA3 c.668G>A - CNGA3_000118 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: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.668G>A r.(?) p.(Arg223Gln) - Parent #2 ACMG pathogenic g.99008428G>A g.98391965G>A CNGA3 c.668G>A - CNGA3_000118 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.668G>A r.(?) p.(Arg223Gln) - Parent #2 ACMG pathogenic g.99008428G>A g.98391965G>A CNGA3 c.668G>A - CNGA3_000118 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: 0, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.668G>A r.(?) p.(Arg223Gln) TM2 Unknown - pathogenic (recessive) g.99008428G>A g.98391965G>A - - CNGA3_000118 ACMG PP5_strong, PP1_sup, PM2_mod, PM5_mod, PP3_sup, PP2_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.668G>A - p.Arg223Gln TM2 Unknown - NA g.99008428G>A g.98391965G>A - - CNGA3_000118 in vitro functional analysis normalized overall luminescence signal (AUC) 0.04±0.01, normalized peak latency 1.76±0.09 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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