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.
Legend   How to query  

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.1627_1635del r.(?) p.(Asp543_Ser545del) - Parent #2 - likely pathogenic (recessive) g.99013260_99013268del g.98396797_98396805del - - CNGA3_000138 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT197 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.1627_1635del r.(?) p.(Asp543_Ser545del) - Parent #2 - likely pathogenic (recessive) g.99013260_99013268del g.98396797_98396805del - - CNGA3_000138 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT858 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.1627_1635del r.(?) p.(Asp543_Ser545del) - Parent #2 - likely pathogenic (recessive) g.99013260_99013268del g.98396797_98396805del - - CNGA3_000138 - PubMed: Huang 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease QT1193 PubMed: Huang 2016 - - - China - - - - - 1 Johan den Dunnen
+/. - c.1627_1635del r.(?) p.(Asp543_Ser545del) - Both (homozygous) - pathogenic g.99013260_99013268del g.98396797_98396805del c.1627_1635del, p.(Asp543_Ser545del) - CNGA3_000138 Homozygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 14401 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.1627_1635del r.(?) p.(Asp543_Ser545del) - Unknown - likely pathogenic g.99013260_99013268del g.98396797_98396805del CNGA3 c.513G>T(;)1627_1635del - CNGA3_000138 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 14792 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. - c.1627_1635del r.(?) p.(Asp543_Ser545del) - Parent #2 - likely pathogenic g.99013260_99013268del g.98396797_98396805del CNGA3 c.[1074G>A];[1627_1635del] - CNGA3_000138 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 19550 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.