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.

7 entries on 1 page. Showing entries 1 - 7.
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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     
+?/. 8 c.1021T>C r.(?) p.(Ser341Pro) - Parent #2 - likely pathogenic g.99012654T>C - p.S341P - CNGA3_000096 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. 7 c.1021T>C r.(?) p.(Ser341Pro) - Parent #2 - likely pathogenic g.99012654T>C g.98396191T>C allele 1/2: R223W/S341P - CNGA3_000096 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO119/M PubMed: Wissinger 2001 - M - Italy - - - - - 1 LOVD
+/. - c.1021T>C r.(?) p.(Ser341Pro) - Parent #1 - pathogenic g.99012654T>C g.98396191T>C CNGA3 allele 1/allele 2: S341P/R277G - CNGA3_000096 heterozygous PubMed: Koeppen 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO367-2641 PubMed: Koeppen 2010 - M - Germany - - - - - 1 LOVD
+/. - c.1021T>C r.(?) p.(Ser341Pro) - Parent #1 ACMG pathogenic g.99012654T>C g.98396191T>C CNGA3 c.1021T>C - CNGA3_000096 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.1021T>C r.(?) p.(Ser341Pro) - Parent #2 ACMG pathogenic g.99012654T>C g.98396191T>C CNGA3 c.1021T>C - CNGA3_000096 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.1021T>C r.(?) p.(Ser341Pro) - Parent #2 ACMG pathogenic g.99012654T>C g.98396191T>C CNGA3 c.1021T>C - CNGA3_000096 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.1021T>C r.(?) p.(Ser341Pro) - Unknown ACMG pathogenic (recessive) g.99012654T>C g.98396191T>C - - CNGA3_000096 ACMG PP3, PM2, PM1, PP2, PP5_STRONG PubMed: Weisschuh 2024 866559 - Germline - - - - - DNA SEQ-NG - WGS ? ACHM-1301 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
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