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.

5 entries on 1 page. Showing entries 1 - 5.
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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.1565T>C r.(?) p.(Ile522Thr) - Unknown - pathogenic g.99013198T>C g.98396735T>C - - CNGA3_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 8 c.1565T>C r.(?) p.(Ile522Thr) - Unknown - likely pathogenic g.99013198T>C - c.1565T>C (p.I522T) - CNGA3_000043 - PubMed: Thiadens_2009 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Thiadens_2009 - - - Netherlands - - - - - 1 LOVD
+?/. 7 c.1565T>C r.(?) p.(Ile522Thr) - Parent #1 - likely pathogenic g.99013198T>C g.98396735T>C allele 1/2: I522T/F547L - CNGA3_000043 heterozygous PubMed: Wissinger 2001 - - Unknown ? - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO171/M PubMed: Wissinger 2001 - M - Netherlands - - - - - 1 LOVD
+?/. - c.1565T>C r.(?) p.(Ile522Thr) - Parent #2 ACMG likely pathogenic g.99013198T>C g.98396735T>C CNGA3 c.1565T>C - CNGA3_000043 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.1565T>C r.(?) p.(Ile522Thr) - Parent #2 ACMG likely pathogenic g.99013198T>C g.98396735T>C CNGA3 c.1565T>C - CNGA3_000043 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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