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.1351dup r.(?) p.(Val451GlyfsTer3) - Parent #1 - pathogenic (recessive) g.99012984dup g.98396521dup 1351dupG - CNGA3_000146 - PubMed: Dubis 2015 - - Germline - - - - - DNA SEQ - - retinal disease JC_1240 PubMed: Dubis 2015 - F - - - - - - - 1 LOVD
+?/. 7 c.1351dup r.(?) p.(Val451Glyfs*3) - Parent #2 - likely pathogenic g.99012984dup g.98396521dup allele 1/2: R427C/V451fs - CNGA3_000146 error in annotation, actual change should be c.1351dup and not 1350insG; heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO38/M PubMed: Wissinger 2001 - F - United States - - - - - 1 LOVD
+?/. - c.1351dup r.(?) p.(Val451Glyfs*3) - Parent #1 - likely pathogenic g.99012984dup g.98396521dup CNGA3 allele 1/allele 2: V451(fs)/R427C - CNGA3_000146 no cDNA annotation given, variant extrapolated from literature PubMed: Koeppen 2008 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO38 PubMed: Koeppen 2008 - F - - - - - - - 1 LOVD
+?/. - c.1351dup r.(?) p.(Val451Glyfs*3) - Parent #2 - likely pathogenic g.99012984dup g.98396521dup c.1279C>T I c.1350insG - CNGA3_000146 heterozygous PubMed: Zelinger 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD2724 PubMed: Zelinger 2015 - - no United States Old Order Amish/British - - - - 1 LOVD
+?/. - c.1351dup r.(?) p.(Val451Glyfs*3) - Parent #2 ACMG likely pathogenic g.99012984dup g.98396521dup CNGA3 c.1351dup - CNGA3_000146 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: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
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