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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
+?/. 7 c.1574G>A r.(?) p.(Gly525Asp) - Parent #1 ACMG likely pathogenic (recessive) g.99013207G>A g.98396744G>A allele 1/2: G525D/T565M - CNGA3_000226 ACMG PP3_strong, PS3_sup, PS4_sup, PM2_sup, PM3_sup PubMed: Wissinger 2001, PubMed: Andersen 2023 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO79/O; Fam209Pat43 PubMed: Wissinger 2001, PubMed: Andersen 2023 sib M - Denmark - - - - - 1 LOVD
+/. - c.1574G>A r.(?) p.(Gly525Asp) - Parent #1 ACMG pathogenic g.99013207G>A g.98396744G>A CNGA3 c.1574G>A - CNGA3_000226 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: 0, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.1574G>A r.(?) p.(Gly525Asp) - Parent #2 ACMG pathogenic g.99013207G>A g.98396744G>A CNGA3 c.1574G>A - CNGA3_000226 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.1574G>A r.(?) p.(Gly525Asp) - Parent #1 ACMG likely pathogenic (recessive) g.99013207G>A g.98396744G>A - - CNGA3_000226 ACMG PP3_strong, PS3_sup, PS4_sup, PM2_sup, PM3_sup PubMed: Andersen 2023 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel ACHM Fam209Pat42 PubMed: Andersen 2023 family, 3 affected - no Denmark - - - - - 3 Susanne Kohl
+?/. - c.1574G>A r.(?) p.(Gly525Asp) - Parent #1 ACMG likely pathogenic (recessive) g.99013207G>A g.98396744G>A - - CNGA3_000226 ACMG PP3_strong, PS3_sup, PS4_sup, PM2_sup, PM3_sup PubMed: Andersen 2023 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel ACHM Fam209Pat96 PubMed: Andersen 2023 sib - no Denmark - - - - - 1 Susanne Kohl
+?/. - c.1574G>A r.(?) p.(Gly525Asp) - Parent #2 ACMG likely pathogenic (recessive) g.99013207G>A g.98396744G>A - - CNGA3_000226 ACMG PP3_strong, PS3_sup, PS4_sup, PM2_sup, PM3_sup PubMed: Andersen 2023 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel ACHM Pat61 PubMed: Andersen 2023 patient - no Denmark - - - - - 1 Susanne Kohl
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