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.101+1G>A r.spl? p.? - Unknown - pathogenic g.98986540G>A g.98370077G>A CNGA3(NM_001298.2):c.101+1G>A - CNGA3_000080 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.101+1G>A r.spl p.? - Unknown ACMG pathogenic g.98986540G>A - - - CNGA3_000080 - 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
+?/. - c.101+1G>A r.spl p.? - Parent #1 - likely pathogenic g.98986540G>A g.98370077G>A IVS2+1G>A - CNGA3_000080 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 456 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+?/. - c.101+1G>A r.spl p.(?) - Both (homozygous) - likely pathogenic g.98986540G>A g.98370077G>A c.101+1G>A - CNGA3_000080 - PubMed: Abdelkader 2018 - - Germline ? - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease 2 PubMed: Abdelkader 2018 - M yes - - - - - - 1 LOVD
+?/. - c.101+1G>A r.spl p.(?) - Both (homozygous) - likely pathogenic g.98986540G>A g.98370077G>A c.101+1G>A - CNGA3_000080 - PubMed: Abdelkader 2018 - - Germline ? - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease 3 PubMed: Abdelkader 2018 - M yes - - - - - - 1 LOVD
+?/. - c.101+1G>A r.spl p.(?) - Both (homozygous) - likely pathogenic g.98986540G>A g.98370077G>A c.101+1G>A - CNGA3_000080 - PubMed: Abdelkader 2018 - - Germline ? - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease 5 PubMed: Abdelkader 2018 - M yes - - - - - - 1 LOVD
+/. - c.101+1G>A r.spl? p.? - Unknown - pathogenic g.98986540G>A - CNGA3(NM_001298.2):c.101+1G>A - CNGA3_000080 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 2i c.101+1G>A r.52_101del p.Val18Serfs*6 - Unknown - NA g.98986540G>A g.98370077G>A - - CNGA3_000080 analysis variant in in vitro mini-gene splicing assay PubMed: Reuter 2021 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+/. 2i c.101+1G>A r.(52_101del) p.(Val18Serfs*6) - Unknown ACMG pathogenic (recessive) g.98986540G>A g.98370077G>A - - CNGA3_000080 effect on RNA predicted from in vitro mini-gene splicing assay; ACMG PS1_Very strong, PM2_Moderate, PP5_Supporting, PP3_supporting, PS3_Strong - VCV000208567 - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. 2i c.101+1G>A r.spl p.Val18Serfs*6 - Parent #1 ACMG pathogenic g.98986540G>A g.98370077G>A - - CNGA3_000080 - PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - Germline - - - - - DNA SEQ, SEQ-NG - smMIP-based 105 iMD/AMD genes macular dystrophy 072215 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - 1 Rebekkah Hitti-Malin
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