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.
Legend   How to query  

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.572G>A r.(?) p.(Cys191Tyr) - Parent #2 - likely pathogenic g.99008332G>A g.98391869G>A - - CNGA3_000110 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 454 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.572G>A r.(?) p.(Cys191Tyr) - Parent #1 - likely pathogenic g.99008332G>A g.98391869G>A CNGA3, variant 1: c.572G>A/p.C191Y, variant 2: c.829C>T/p.R277C - CNGA3_000110 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1299 PubMed: Weisschuh 2020 Filing key number: 1159, achromatopsia, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 6 c.572G>A r.(?) p.(Cys191Tyr) - Parent #1 - likely pathogenic g.99008332G>A g.98391869G>A allele 1/2: C191Y/R277C - CNGA3_000110 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO118/399 PubMed: Wissinger 2001 - M - Germany - - - - - 1 LOVD
+?/. 6 c.572G>A r.(?) p.(Cys191Tyr) - Both (homozygous) - likely pathogenic g.99008332G>A g.98391869G>A allele 1/2: C191Y/C191Y - CNGA3_000110 homozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO241/7-1 PubMed: Wissinger 2001 - M - Italy - - - - - 1 LOVD
+?/. - c.572G>A r.(?) p.(Cys191Tyr) - Parent #2 ACMG likely pathogenic g.99008332G>A g.98391869G>A CNGA3 c.572G>A - CNGA3_000110 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.572G>A r.(?) p.(Cys191Tyr) - Both (homozygous) ACMG likely pathogenic g.99008332G>A g.98391869G>A CNGA3 c.572G>A - CNGA3_000110 homozygous 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.572G>A r.(?) p.(Cys191Tyr) - Parent #1 ACMG likely pathogenic g.99008332G>A g.98391869G>A CNGA3 c.572G>A - CNGA3_000110 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.572G>A r.(?) p.(Cys191Tyr) - Parent #1 ACMG likely pathogenic g.99008332G>A g.98391869G>A CNGA3 c.572G>A - CNGA3_000110 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.572G>A r.(?) p.(Cys191Tyr) - Parent #1 ACMG likely pathogenic g.99008332G>A g.98391869G>A CNGA3 c.572G>A - CNGA3_000110 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.572G>A r.(?) p.(Cys191Tyr) - Parent #2 ACMG likely pathogenic g.99008332G>A g.98391869G>A CNGA3 c.572G>A - CNGA3_000110 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 2 ; number of affected individuals: 2; segregation analysis: both parents: 0, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.