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.

22 entries on 1 page. Showing entries 1 - 22.
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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.661C>T r.(?) p.(Arg221Ter) - Unknown - pathogenic g.99008421C>T g.98391958C>T - - CNGA3_000063 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 7 c.661C>T r.(?) p.(Arg221*) - Both (homozygous) - pathogenic (recessive) g.99008421C>T - Arg221Stop/Arg221Stop - CNGA3_000063 - PubMed: Johnson 2004 - - Germline - - - - - DNA SEQ Blood - retinal disease - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - 1 Julia Lopez
+/. - c.661C>T r.(?) p.(Arg221*) - Parent #1 - pathogenic (recessive) g.99008421C>T g.98391958C>T - - CNGA3_000063 - PubMed: Matet 2018 - - Germline - - - - - DNA SEQ - - retinal disease Pat7 PubMed: Matet 2018 - M no - white - - - - 1 LOVD
+?/. - c.661C>T r.(?) p.(Arg221Ter) - Parent #1 - likely pathogenic (recessive) g.99008421C>T g.98391958C>T - - CNGA3_000063 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT199 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.661C>T r.(?) p.(Arg221Ter) - Parent #1 - likely pathogenic (recessive) g.99008421C>T g.98391958C>T - - CNGA3_000063 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT415 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.661C>T r.(?) p.(Arg221Ter) - Parent #2 - likely pathogenic (recessive) g.99008421C>T g.98391958C>T - - CNGA3_000063 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT660 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.661C>T r.(?) p.(Arg221Ter) - Unknown - likely pathogenic g.99008421C>T g.98391958C>T - - CNGA3_000063 - PubMed: Patel 2016 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease 12DG0442 PubMed: Patel 2016 - - - Saudi Arabia - - - - - 1 LOVD
?/. 7 c.661C>T r.(?) p.(Arg221*) - Both (homozygous) - VUS g.99008421C>T - c.661C>T - CNGA3_000063 - PubMed: Abu-Safieh-2013 - - Germline - - - - - DNA SEQ-NG blood autozygome-guided sequencing retinal disease - PubMed: Abu-Safieh-2013 - - - Saudi Arabia - - - - - 1 LOVD
+?/. - c.661C>T r.(?) p.(Arg221*) - Both (homozygous) - likely pathogenic g.99008421C>T g.98391958C>T c.661C>T; p.(Arg221*) - CNGA3_000063 - PubMed: Abdelkader 2018 - - Germline ? - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease 2 PubMed: Abdelkader 2018 - M yes - - - - - - 1 LOVD
+?/. - c.661C>T r.(?) p.(Arg221*) - Both (homozygous) - likely pathogenic g.99008421C>T g.98391958C>T c.661C>T; p.(Arg221*) - CNGA3_000063 - PubMed: Abdelkader 2018 - - Germline ? - - - - DNA SEQ-NG blood Whole-exome sequencing retinal disease 3 PubMed: Abdelkader 2018 - M yes - - - - - - 1 LOVD
+/. 7 c.661C>T r.(?) p.(Arg221*) - Unknown - pathogenic g.99008421C>T - c.661C>T - CNGA3_000063 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - F - - - - - - - 1 Julia Lopez
+/. 7 c.661C>T r.(?) p.(Arg221*) - Both (homozygous) - pathogenic g.99008421C>T - c.661C>T - CNGA3_000063 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - F - - - - - - - 1 Julia Lopez
+/. 7 c.661C>T r.(?) p.(Arg221*) - Unknown - pathogenic g.99008421C>T - c.661C>T - CNGA3_000063 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - F - - - - - - - 1 Julia Lopez
+/. 7 c.661C>T r.(?) p.(Arg221*) - Unknown - pathogenic g.99008421C>T - c.661C>T - CNGA3_000063 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - M - - - - - - - 1 Julia Lopez
+/. - c.661C>T r.(?) p.(Arg221*) - Unknown - pathogenic g.99008421C>T g.98391958C>T c.661C>T, p.(Arg221*) - CNGA3_000063 compound heterozygous PubMed: Wang 2019 - - Germline yes - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13681 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.661C>T r.(?) p.(Arg221*) - Parent #1 - likely pathogenic g.99008421C>T g.98391958C>T CNGA3 c.[661C>T];[830G>A] - CNGA3_000063 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 11902 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. 6 c.661C>T r.(?) p.(Arg221*) - Parent #1 - likely pathogenic g.99008421C>T g.98391958C>T allele 1: c.661C>T - p.Arg221Stop, allele 2: c.830G>A - p.Arg277His - CNGA3_000063 heterozygous PubMed: Genead 2011 - - Unknown ? - - - - DNA SEQ blood - retinal disease 2 PubMed: Genead 2011 - M - United States white - - - - 1 LOVD
+?/. - c.661C>T r.(?) p.(Arg221*) - Unknown - likely pathogenic g.99008421C>T g.98391958C>T CNGA3 c.661C>T, (p.Arg221*) - CNGA3_000063 - PubMed: Matet 2018 - - Unknown ? - - - - DNA SEQ-NG - tagreted next-generation sequencing retinal disease 7 PubMed: Matet 2018 - M no France white - - - - 1 LOVD
+?/. p.(Arg221Ter) c.661C>T r.(?) p.(Arg221Ter) - Both (homozygous) - likely pathogenic g.99008421C>T g.98391958C>T CNGA3 661C>T, Arg221Ter - CNGA3_000063 homozygous PubMed: Georgiou 2019 - - Unknown ? - - - - DNA ? - retrospective research retinal disease MM_0418 PubMed: Georgiou 2019 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.661C>T r.(?) p.(Arg221*) - Parent #2 ACMG pathogenic g.99008421C>T g.98391958C>T CNGA3 c.661C>T - CNGA3_000063 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: 1; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.661C>T r.(?) p.(Arg221*) - Parent #1 ACMG pathogenic g.99008421C>T g.98391958C>T CNGA3 c.661C>T - CNGA3_000063 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.661C>T r.(?) p.(Arg221*) - Parent #2 ACMG pathogenic g.99008421C>T g.98391958C>T CNGA3 c.661C>T - CNGA3_000063 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
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