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.107_110del r.(?) p.(His36Argfs*136) - Parent #1 - pathogenic g.98994155_98994158del g.98377692_98377695del 107_110delACTC - CNGA3_000112 - PubMed: Carrigan 2016 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease - PubMed: Carrigan 2016 - - - Ireland - - - - - 1 LOVD
+?/. - c.107_110del r.(?) p.(His36Argfs*136) - Unknown - likely pathogenic g.98994155_98994158del g.98377692_98377695del CNGA3 c.107_110delACTC, p.His36ArgfsTer136 - CNGA3_000112 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G006297 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.107_110del r.(?) p.(His36Argfs*136) - Parent #2 - likely pathogenic g.98994155_98994158del g.98377692_98377695del allele 1: c.1279C>T, p.R427C, allele 2: c.107_110del, p.H36RfsX118 - CNGA3_000112 heterozygous PubMed: Thomas 2012 - - Unknown ? - - - - DNA SEQ blood - retinal disease 1 PubMed: Thomas 2012 - ? yes - - - - - - 1 LOVD
+?/. - c.107_110del r.(?) p.(His36Argfs*136) - Parent #2 - likely pathogenic g.98994155_98994158del g.98377692_98377695del allele 1: c.1279C>T, p.R427C, allele 2: c.107_110del, p.H36RfsX118 - CNGA3_000112 heterozygous PubMed: Thomas 2012 - - Unknown ? - - - - DNA SEQ blood - retinal disease 2 PubMed: Thomas 2012 - ? yes - - - - - - 1 LOVD
+/. - c.107_110del r.(?) p.(His36Argfs*136) - Parent #2 ACMG pathogenic g.98994155_98994158del g.98377692_98377695del CNGA3 c.107_110del - CNGA3_000112 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 2; segregation analysis: both parents: 2, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
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