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.

14 entries on 1 page. Showing entries 1 - 14.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.682G>A r.(?) p.(Glu228Lys) - Unknown - VUS g.99012315G>A g.98395852G>A CNGA3(NM_001079878.1):c.628G>A (p.(Glu210Lys)) - CNGA3_000016 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.682G>A r.(?) p.(Glu228Lys) - Parent #1 - VUS g.99012315G>A g.98395852G>A - - CNGA3_000016 conflicting interpretations of pathogenicity; 64 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs147415641 Germline - 64/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 64 Mohammed Faruq
?/. - c.682G>A r.(?) p.(Glu228Lys) - Both (homozygous) - VUS g.99012315G>A g.98395852G>A - - CNGA3_000016 conflicting interpretations of pathogenicity; 1 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs147415641 Germline - 1/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+?/. - c.682G>A r.(?) p.(Glu228Lys) - Unknown ACMG likely pathogenic g.99012315G>A - - - CNGA3_000016 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+?/. 8 c.682G>A r.(?) p.(Glu228Lys) - Unknown - likely pathogenic g.99012315G>A - c.682G>A (p.E228K) - CNGA3_000016 - PubMed: Thiadens_2010 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Thiadens_2010 - M - Netherlands - - - - - 1 LOVD
+?/. - c.682G>A r.(?) p.(Glu228Lys) - Parent #1 - likely pathogenic g.99012315G>A g.98395852G>A CNGA3, variant 1 :[c.682G>A/p.E228K; c.1315C>T/p.R439W], variant 2 :[c.682G>A/p.E228K; c.1315C>T/p.R439W] - CNGA3_000016 solved, homozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 1122 PubMed: Weisschuh 2020 Filing key number: 767, achromatopsia, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.682G>A r.(?) p.(Glu228Lys) - Parent #1 - likely pathogenic g.99012315G>A g.98395852G>A CNGA3, variant 1 :[c.682G>A/p.E228K; c.1315C>T/p.R439W], variant 2 :[c.682G>A/p.E228K; c.1315C>T/p.R439W] - CNGA3_000016 solved, homozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 1123 PubMed: Weisschuh 2020 Filing key number: 767, achromatopsia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.682G>A r.(?) p.(Glu228Lys) - Both (homozygous) - likely pathogenic g.99012315G>A g.98395852G>A allele 1/2: E228K/E228K - CNGA3_000016 homozygous PubMed: Reuter 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO335-1 PubMed: Reuter 2008 - M - Germany - - - - - 1 LOVD
+?/. - c.682G>A r.(?) p.(Glu228Lys) - Both (homozygous) - likely pathogenic g.99012315G>A g.98395852G>A allele 1/2: E228K/E228K - CNGA3_000016 homozygous PubMed: Reuter 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO335-2 PubMed: Reuter 2008 - M - Germany - - - - - 1 LOVD
+?/. - c.682G>A r.(?) p.(Glu228Lys) - Parent #1 ACMG likely pathogenic g.99012315G>A g.98395852G>A - - CNGA3_000016 - PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - - Germline - - - - - DNA MIPsm - smMIPs 105 iMD/AMD genes retinal disease 070241 PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - F - - - - - - - 1 Rebekkah Hitti-Malin
+/. - c.682G>A r.(?) p.(Glu228Lys) - Both (homozygous) ACMG pathogenic g.99012315G>A g.98395852G>A CNGA3 c.[67C>T;682G>A] - CNGA3_000016 homozygous PubMed: Solaki 2022 - - Unknown ? - - - - 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.682G>A r.(?) p.(Glu228Lys) - Both (homozygous) ACMG pathogenic g.99012315G>A g.98395852G>A CNGA3 c.[682G>A;1315C>T] - CNGA3_000016 homozygous 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
+?/. 8 c.682G>A r.(?) p.(Glu228Lys) - Parent #1 ACMG likely pathogenic g.99012315G>A g.98395852G>A - - CNGA3_000016 - PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - Germline - - - - - DNA SEQ, SEQ-NG - smMIP-based 105 iMD/AMD genes macular dystrophy 072180 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - M - - - - - - - 1 Rebekkah Hitti-Malin
+/. - c.682G>A r.682G>A p.Glu228Lys - Unknown ACMG pathogenic g.99012315G>A g.98395852G>A - - CNGA3_000016 possible digenic, triallelic inheritance Rawnsley 2025, submitted - - Germline - - - - - DNA SEQ - - ACHM3 CHRO1238 Rawnsley 2025, submitted - - - Germany - - - - - 1 Susanne Kohl
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