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.

15 entries on 1 page. Showing entries 1 - 15.
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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     

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VIP     

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Owner     
?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown - VUS g.99013251G>A g.98396788G>A CNGA3(NM_001298.2):c.1618G>A (p.V540I), CNGA3(NM_001298.3):c.1618G>A (p.V540I) - CNGA3_000021 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown - likely benign g.99013251G>A g.98396788G>A CNGA3(NM_001298.2):c.1618G>A (p.V540I), CNGA3(NM_001298.3):c.1618G>A (p.V540I) - CNGA3_000021 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1618G>A r.(?) p.(Val540Ile) - Parent #1 - VUS g.99013251G>A g.98396788G>A - - CNGA3_000021 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs116448158 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown ACMG likely pathogenic g.99013251G>A - - - CNGA3_000021 - 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.1618G>A r.(?) p.(Val540Ile) - Unknown - VUS g.99013251G>A g.98396788G>A - - CNGA3_000021 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case71927 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - 1 LOVD
+?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown - likely pathogenic g.99013251G>A g.98396788G>A - - CNGA3_000021 - PubMed: Patel 2016 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease 11DG2411 PubMed: Patel 2016 - - - Saudi Arabia - - - - - 1 LOVD
+?/. 8 c.1618G>A r.(?) p.(Val540Ile) - Unknown - likely pathogenic g.99013251G>A - c.1618G>A (p.V540I) - CNGA3_000021 - PubMed: Thiadens_2010 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Thiadens_2010 - - - Netherlands - - - - - 1 LOVD
?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown ACMG VUS g.99013251G>A g.98396788G>A CNGA3:NM_001298 c.G1618A, p.V540I - CNGA3_000021 heterozygous, individual solved, variant non-causal PubMed: Rodriguez-Munoz 2020 - - Germline ? - - - - DNA SEQ-NG-I blood - retinal disease RPN-125 PubMed: Rodriguez-Munoz 2020 family fRPN-50, proband F - Spain - - - - - 1 LOVD
?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown - VUS g.99013251G>A g.98396788G>A CNGA3 nucleotide 1, protein 1:c.1148delC, p.Thr383Ilefs*13 nucleotide 2, protein 2:c.1618>A:p., p.(Val540Ile) - CNGA3_000021 heterozygous, ACMG unclassified - no access to supplementary table 2 PubMed: Hull 2020 - - Germline ? - - - - DNA ? blood NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families retinal disease 43 PubMed: Hull 2020 - ? - New Zealand white - - - - 1 LOVD
?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown - VUS g.99013251G>A - - - CNGA3_000021 - PubMed: Langlo 2014 - - Germline - - - - - DNA SEQ - - retinal disease PCI-012 PubMed: Langlo 2014 - F - United States - - - - - 1 Johan den Dunnen
-?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown - likely benign g.99013251G>A - CNGA3(NM_001298.2):c.1618G>A (p.V540I), CNGA3(NM_001298.3):c.1618G>A (p.V540I) - CNGA3_000021 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1618G>A r.(?) p.(Val540Ile) - Unknown ACMG VUS g.99013251G>A g.98396788G>A - - CNGA3_000021 ACMG PM2, PP2, PP5; no variant 2nd chromosome PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? SRP-288 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
-/. - c.1618G>A r.(?) p.(Val540Ile) CNBD β5 Unknown - benign g.99013251G>A g.98396788G>A - - CNGA3_000021 ACMG BS1_strong, PM1_sup, PP2_sup, PP3_sup, BS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.1618G>A - p.Val540Ile CNBD β5 Unknown - NA g.99013251G>A g.98396788G>A - - CNGA3_000021 in vitro functional analysis normalized overall luminescence signal (AUC) 0.74±0.05, normalized peak latency 0.96±0.03 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+?/. 8 c.1618G>A r.(?) p.(Val540Ile) - Parent #2 ACMG likely pathogenic g.99013251G>A g.98396788G>A - - CNGA3_000021 - PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - Germline - - - - - DNA SEQ, SEQ-NG - smMIP-based 105 iMD/AMD genes macular dystrophy 066749 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - M - - - - - - - 1 Rebekkah Hitti-Malin
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