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.

17 entries on 1 page. Showing entries 1 - 17.
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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.778G>A r.(?) p.(Asp260Asn) - Parent #2 - likely pathogenic (recessive) g.99012411G>A g.98395948G>A - - CNGA3_000122 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT425 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. 8 c.778G>A r.(?) p.(Asp260Asn) - Unknown - likely pathogenic g.99012411G>A - c.778G>A (p.D260N) - CNGA3_000122 - PubMed: Thiadens_2009 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Thiadens_2009 - - - Netherlands - - - - - 1 LOVD
+?/. - c.778G>A r.(?) p.(Asp260Asn) - Parent #1 - likely pathogenic g.99012411G>A g.98395948G>A CNGA3, variant 1: c.1641C>A/p.F547L, variant 2: c.778G>A/p.D260N - CNGA3_000122 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 530 PubMed: Weisschuh 2020 Filing key number: 180, achromatopsia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. 7 c.778G>A r.(?) p.(Asp260Asn) - Parent #2 - likely pathogenic g.99012411G>A g.98395948G>A allele 1/2: D162V/D260N - CNGA3_000122 heterozygous PubMed: Wissinger 2001 - - Unknown ? - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO135/H PubMed: Wissinger 2001 - M - Netherlands - - - - - 1 LOVD
+?/. - c.778G>A r.(?) p.(Asp260Asn) - Unknown - likely pathogenic g.99012411G>A g.98395948G>A CNGA3 heterozygous p.D260N:c.778G>A; CNGB3 heterozygous c.1148delC, p.R403Q:c.1208G>A - CNGA3_000122 - PubMed: Yang 2014 - - Unknown ? - - - - DNA SEQ blood - retinal disease 1 PubMed: Yang 2014 - M - - - - - - - 1 LOVD
+?/. - c.778G>A r.(?) p.(Asp260Asn) - Parent #2 - likely pathogenic g.99012411G>A g.98395948G>A c.829C>T I c.778G>A - CNGA3_000122 heterozygous PubMed: Zelinger 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD3206 PubMed: Zelinger 2015 - - no United States Eastern European - - - - 1 LOVD
+?/. - c.778G>A r.(?) p.(Asp260Asn) - Parent #1 - likely pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A, p.D260N* - CNGA3_000122 heterozygous PubMed: Liang 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease F3-II1 PubMed: Liang 2015 - F - China - - - - - 1 LOVD
+?/. p.(Asp260Asn) c.778G>A r.(?) p.(Asp260Asn) - Parent #2 - likely pathogenic g.99012411G>A g.98395948G>A CNGA3 778G>A, Asp260Asn - CNGA3_000122 heterozygous PubMed: Georgiou 2019 - - Unknown ? - - - - DNA ? - retrospective research retinal disease JC_0578 PubMed: Georgiou 2019 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.778G>A r.(?) p.(Asp260Asn) - Parent #2 ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 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.778G>A r.(?) p.(Asp260Asn) - Parent #2 ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 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.778G>A r.(?) p.(Asp260Asn) - Both (homozygous) ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 homozygous 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: 0, one parent or other relatives: 1; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.778G>A r.(?) p.(Asp260Asn) - Parent #1 ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 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.778G>A r.(?) p.(Asp260Asn) - Parent #1 ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 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.778G>A r.(?) p.(Asp260Asn) - Parent #1 ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 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.778G>A r.(?) p.(Asp260Asn) - Parent #2 ACMG pathogenic g.99012411G>A g.98395948G>A CNGA3 c.778G>A - CNGA3_000122 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: 0, one parent or other relatives: 1; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+?/. - c.778G>A r.(?) p.(Asp260Asn) - Unknown ACMG likely pathogenic (recessive) g.99012411G>A g.98395948G>A - - CNGA3_000122 ACMG PP3, PM2, PP2, PP5_STRONG PubMed: Weisschuh 2024 689726 - Germline - - - - - DNA SEQ-NG - WGS ? ACHM-1298 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
+?/. 8 c.778G>A r.(?) p.(Asp260Asn) - Parent #2 ACMG likely pathogenic g.99012411G>A g.98395948G>A - - CNGA3_000122 - PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - Germline - - - - - DNA SEQ, SEQ-NG - smMIP-based 105 iMD/AMD genes macular dystrophy 072215 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - 1 Rebekkah Hitti-Malin
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