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.

9 entries on 1 page. Showing entries 1 - 9.
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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.542A>G r.(?) p.(Tyr181Cys) - Unknown - likely pathogenic g.99006213A>G g.98389750A>G CNGA3(NM_001298.2):c.542A>G (p.Y181C), CNGA3(NM_001298.3):c.542A>G (p.Y181C) - CNGA3_000012 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.542A>G r.(?) p.(Tyr181Cys) - Unknown - likely pathogenic g.99006213A>G g.98389750A>G CNGA3(NM_001298.2):c.542A>G (p.Y181C), CNGA3(NM_001298.3):c.542A>G (p.Y181C) - CNGA3_000012 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.542A>G r.(?) p.(Tyr181Cys) - Both (homozygous) - pathogenic (recessive) g.99006213A>G g.98389750A>G - - CNGA3_000012 - PubMed: Matet 2018 - - Germline - - - - - DNA SEQ - - retinal disease Pat5 PubMed: Matet 2018 - F yes - Africa-North - - - - 1 LOVD
+?/. - c.542A>G r.(?) p.(Tyr181Cys) - Parent #1 - likely pathogenic g.99006213A>G g.98389750A>G CNGA3 c.[542A>G];[1585G>A] - CNGA3_000012 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 11062 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. 5 c.542A>G r.(?) p.(Tyr181Cys) - Both (homozygous) - likely pathogenic g.99006213A>G g.98389750A>G allele 1/2: Y181C/Y181C - CNGA3_000012 homozygous PubMed: Wissinger 2001 - - Unknown ? - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO179/U PubMed: Wissinger 2001 - M - Germany - - - - - 1 LOVD
+?/. - c.542A>G r.(?) p.(Tyr181Cys) - Unknown - likely pathogenic g.99006213A>G g.98389750A>G CNGA3 c.542A>G, (p.Tyr181Cys) - CNGA3_000012 - PubMed: Matet 2018 - - Unknown ? - - - - DNA SEQ-NG - tagreted next-generation sequencing retinal disease 5 PubMed: Matet 2018 - F yes France Northern African - - - - 1 LOVD
+?/. - c.542A>G r.(?) p.(Tyr181Cys) - Unknown - likely pathogenic g.99006213A>G g.98389750A>G CNGA3 c.542A>G, (p.Tyr181Cys) - CNGA3_000012 - PubMed: Matet 2018 - - Unknown ? - - - - DNA SEQ-NG - tagreted next-generation sequencing retinal disease 5 PubMed: Matet 2018 - F yes France Northern African - - - - 1 LOVD
+/. - c.542A>G r.(?) p.(Tyr181Cys) - Both (homozygous) ACMG pathogenic g.99006213A>G g.98389750A>G CNGA3 c.542A>G - CNGA3_000012 homozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 3 ; number of affected individuals: 3; segregation analysis: both parents: 0, one parent or other relatives: 1; no segregation analysis possible: 2 - - - - - - - - 1 LOVD
+/. - c.542A>G r.(?) p.(Tyr181Cys) - Parent #1 ACMG pathogenic g.99006213A>G g.98389750A>G CNGA3 c.542A>G - CNGA3_000012 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
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