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.

3 entries on 1 page. Showing entries 1 - 3.
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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.-37-1G>C r.spl? p.? - Unknown - pathogenic g.98986401G>C g.98369938G>C CNGA3(NM_001298.3):c.-37-1G>C - CNGA3_000078 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.-37-1G>C r.spl? p.? - Unknown - likely pathogenic g.98986401G>C - CNGA3(NM_001298.3):c.-37-1G>C - CNGA3_000078 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.-37-1G>C r.spl p.(?) - Unknown - pathogenic g.98986401G>C g.98369938G>C CNGB3: c.[1208G>A];[(1208G>A)], p.[R403Q];[(R403Q)], CNGA3: c.[-37-1G>C];[=] - CNGA3_000078 - PubMed: Burkhard 2018 - - Germline ? - - - - DNA SEQ-NG, SEQ blood - retinal disease 7 PubMed: Burkhard 2018 - F no - - - - - - 1 LOVD
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