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.

12 entries on 1 page. Showing entries 1 - 12.
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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     
+?/. 8 c.1768G>A r.(?) p.(Glu590Lys) - Both (homozygous) ACMG VUS g.99013401G>A g.98396938G>A - - CNGA3_000005 - PubMed: de Castro-Miró 2016 - - Germline - - - - - DNA SEQ-NG-I Whole blood - ACHM 75ORG1 PubMed: de Castro-Miró 2016 - F yes Saudi Arabia - - - - - 1 Marta de Castro-Miró
+?/. 8 c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 - likely pathogenic g.99013401G>A - p.E590K - CNGA3_000005 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. 8 c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 - likely pathogenic g.99013401G>A - p.E590K - CNGA3_000005 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. 8 c.1768G>A r.(?) p.(Glu590Lys) - Parent #1 - likely pathogenic g.99013401G>A - p.E590K - CNGA3_000005 - PubMed: Nishiguchi 2005 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Nishiguchi 2005 - - - - - - - - - 1 Julia Lopez
+?/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 - likely pathogenic (recessive) g.99013401G>A g.98396938G>A - - CNGA3_000005 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT7 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 - likely pathogenic (recessive) g.99013401G>A g.98396938G>A - - CNGA3_000005 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT189 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 - likely pathogenic (recessive) g.99013401G>A g.98396938G>A - - CNGA3_000005 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT353 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 - likely pathogenic (recessive) g.99013401G>A g.98396938G>A - - CNGA3_000005 - PubMed: Huang 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease QT1270 PubMed: Huang 2016 - - - China - - - - - 1 Johan den Dunnen
+?/. - c.1768G>A r.(?) p.(Glu590Lys) - Unknown - likely pathogenic g.99013401G>A g.98396938G>A c.1768G>A, p.(Glu590Lys) - CNGA3_000005 compound heterozygous PubMed: Wang 2019 - - Germline yes - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13150 PubMed: Wang 2019 - F - China - - - - - 1 LOVD
+/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 ACMG pathogenic g.99013401G>A g.98396938G>A CNGA3 c.1768G>A - CNGA3_000005 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: 0, one parent or other relatives: 0; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
+/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 ACMG pathogenic g.99013401G>A g.98396938G>A CNGA3 c.1768G>A - CNGA3_000005 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - 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
+/. - c.1768G>A r.(?) p.(Glu590Lys) - Parent #2 ACMG pathogenic g.99013401G>A g.98396938G>A CNGA3 c.1768G>A - CNGA3_000005 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: 0, one parent or other relatives: 0; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
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