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.

19 entries on 1 page. Showing entries 1 - 19.
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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     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.67C>T r.(?) p.(Arg23Ter) - Unknown - pathogenic g.98986505C>T g.98370042C>T - - CNGA3_000028 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 1 c.67C>T r.(?) p.(Arg23*) - Both (homozygous) - pathogenic g.98986505C>T g.98370042C>T - - CNGA3_000028 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - F yes Israel Druze - - - - 5 Dror Sharon
+/. - c.67C>T r.(?) p.(Arg23*) - Unknown ACMG pathogenic g.98986505C>T - - - CNGA3_000028 - PubMed: Sharon 2019 - - Germline - 3/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 3 IRD families - - Israel - - - - - 3 Global Variome, with Curator vacancy
+/. 2 c.67C>T r.(?) p.(Arg23*) - Both (homozygous) - pathogenic (recessive) g.98986505C>T - Arg23Stop/Arg23Stop - CNGA3_000028 - PubMed: Johnson 2004 - - Germline - - - - - DNA SEQ Blood - retinal disease - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - 1 Julia Lopez
+?/. - c.67C>T r.(?) p.(Arg23*) - Unknown - likely pathogenic g.98986505C>T g.98370042C>T - - CNGA3_000028 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 11011667 PubMed: Ellingford 2016 familial segregation analysis requested - - - - - - - - 1 LOVD
+?/. - c.67C>T r.(?) p.(Arg23Ter) - Parent #1 - likely pathogenic (recessive) g.98986505C>T g.98370042C>T - - CNGA3_000028 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT425 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+/. 2 c.67C>T r.(?) p.(Arg23*) - Unknown - pathogenic g.98986505C>T - c.67C>T - CNGA3_000028 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - M - - - - - - - 1 Julia Lopez
+/. 2 c.67C>T r.(?) p.(Arg23*) - Both (homozygous) - pathogenic g.98986505C>T - c.67C>T - CNGA3_000028 - PubMed: Sundaram_2014 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Sundaram_2014 - F - - - - - - - 1 Julia Lopez
+?/. - c.67C>T r.(?) p.(Arg23*) - Paternal (confirmed) - likely pathogenic g.98986505C>T g.98370042C>T c.1279C-->T, c.67C-->T; p.Arg427Cys, p.Arg23* - CNGA3_000028 confirmed with Sanger sequencing; compound heterozygous PubMed: Patel 2019 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - ACHM2 278 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.67C>T r.(?) p.(Arg23*) - Parent #1 - likely pathogenic g.98986505C>T g.98370042C>T CNGA3 allele 1/allele 2: R23X/R427C - CNGA3_000028 no cDNA annotation given, variant extrapolated from literature PubMed: Koeppen 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease ZD212 PubMed: Koeppen 2008 - M - - - - - - - 1 LOVD
+?/. - c.67C>T r.(?) p.(Arg23Ter) - Parent #2 - likely pathogenic g.98986505C>T g.98370042C>T allele 1/2: F547L/R23X - CNGA3_000028 heterozygous PubMed: Reuter 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO440 PubMed: Reuter 2008 - F - Germany - - - - - 1 LOVD
+?/. - c.67C>T r.(?) p.(Arg23Ter) - Both (homozygous) - likely pathogenic g.98986505C>T g.98370042C>T c.67C>T I c.67C>T - CNGA3_000028 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0178-4 PubMed: Zelinger 2015 - - yes Israel Druze - - - - 1 LOVD
+?/. - c.67C>T r.(?) p.(Arg23Ter) - Both (homozygous) - likely pathogenic g.98986505C>T g.98370042C>T c.67C>T I c.67C>T - CNGA3_000028 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0909-1 PubMed: Zelinger 2015 - - yes Israel Druze - - - - 1 LOVD
+/. - c.67C>T r.(?) p.(Arg23*) - Both (homozygous) ACMG pathogenic g.98986505C>T g.98370042C>T CNGA3 c.[67C>T;682G>A] - CNGA3_000028 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: 0, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.67C>T r.(?) p.(Arg23*) - Parent #2 ACMG pathogenic g.98986505C>T g.98370042C>T CNGA3 c.67C>T - CNGA3_000028 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.67C>T r.(?) p.(Arg23*) - Parent #2 ACMG pathogenic g.98986505C>T g.98370042C>T CNGA3 c.67C>T - CNGA3_000028 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - 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.67C>T r.(?) p.(Arg23*) - Parent #1 ACMG pathogenic g.98986505C>T g.98370042C>T CNGA3 c.67C>T - CNGA3_000028 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: 2, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.67C>T r.(?) p.(Arg23*) - Parent #1 ACMG pathogenic g.98986505C>T g.98370042C>T CNGA3 c.67C>T - CNGA3_000028 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - 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.67C>T r.(?) p.(Arg23Ter) - Parent #1 ACMG pathogenic (recessive) g.98986505C>T g.98370042C>T - - CNGA3_000028 ACMG PVS1, PS4_moderate, PM2_sup PubMed: Andersen 2023 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel ACHM Pat76 PubMed: Andersen 2023 patient - no Denmark - - - - - 1 Susanne Kohl
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