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.

26 entries on 1 page. Showing entries 1 - 26.
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.1100G>T r.(?) p.(Gly367Val) - Both (homozygous) ACMG pathogenic g.99012733G>T g.98396270G>T CNGA3 c.1100G>T - CNGA3_000036 homozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 3 ; number of affected individuals: 4; segregation analysis: both parents: 3, one parent or other relatives: 0; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Unknown - likely pathogenic g.99012747C>T g.98396284C>T - - CNGA3_000036 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 7 c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic g.99012747C>T g.98396284C>T - - CNGA3_000036 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - M yes Israel Beduin - - - - 2 Dror Sharon
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Unknown ACMG pathogenic g.99012747C>T - - - CNGA3_000036 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Unknown ACMG pathogenic g.99012747C>T - - - CNGA3_000036 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic (recessive) g.99012747C>T g.98396284C>T NM_001079878:c.1060C>T - CNGA3_000036 - PubMed: DiIorio 2017 - - Germline - - - - - DNA SEQ-NG - 150-gene panel retinal disease Pat40 PubMed: Di Iorio 2017 - - - Italy - - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Parent #2 - likely pathogenic g.99012747C>T g.98396284C>T - - CNGA3_000036 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 455 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic g.99012747C>T g.98396284C>T Allele 1 c.1114C>T (p.Pro372Ser), Allele 2 c.1114C>T (p.Pro372Ser) - CNGA3_000036 homozygous PubMed: Khan 2019 - - Germline/De novo (untested) ? - - - - DNA ? - retrospective study retinal disease - PubMed: Khan 2019 - M - - - - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic g.99012747C>T g.98396284C>T CNGA3 c.[1114C > T];[1114C > T], p.[P372S];[P372S] - CNGA3_000036 homozygous PubMed: Habibi 2020 - - Germline ? - - - - DNA SEQ-NG-I blood whole exome sequencing retinal disease F24_II.3 PubMed: Habibi 2020 Family F24, patient II.3 M - Tunisia - - - - - 1 LOVD
?/. 8 c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - VUS g.99012747C>T - c.1114C>T - CNGA3_000036 - PubMed: Brunetti-Pierri_2021 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Brunetti-Pierri_2021 - - no - Italian - - - - 1 LOVD
?/. 8 c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - VUS g.99012747C>T - c.1114C>T - CNGA3_000036 - PubMed: Brunetti-Pierri_2021 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Brunetti-Pierri_2021 - - no - Italian - - - - 1 LOVD
+?/. 7 c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic g.99012747C>T g.98396284C>T allele 1/2: P372S/P372S - CNGA3_000036 homozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO121/N PubMed: Wissinger 2001 - F - Tunisia - - - - - 1 LOVD
+?/. 7 c.1114C>T r.(?) p.(Pro372Ser) - Parent #2 - likely pathogenic g.99012747C>T g.98396284C>T allele 1/2: R283W/P372S - CNGA3_000036 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO124/C PubMed: Wissinger 2001 - F - Germany - - - - - 1 LOVD
+?/. 7 c.1114C>T r.(?) p.(Pro372Ser) - Parent #2 - likely pathogenic g.99012747C>T g.98396284C>T allele 1/2: R283W/P372S - CNGA3_000036 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO124/T PubMed: Wissinger 2001 - M - Germany - - - - - 1 LOVD
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - pathogenic g.99012733G>T g.98396270G>T CNGA3 allele 1/allele 2: P372S/P372S - CNGA3_000036 homozygous PubMed: Koeppen 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO532-16588 PubMed: Koeppen 2010 - F - Germany - - - - - 1 LOVD
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - pathogenic g.99012747C>T g.98396284C>T CNGA3 allele 1/allele 2: P372S/P372S - CNGA3_000036 homozygous PubMed: Koeppen 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO544-16904 PubMed: Koeppen 2010 - F - Germany - - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic g.99012747C>T g.98396284C>T c.1114C>T I c.1114C>T - CNGA3_000036 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0294-1 PubMed: Zelinger 2015 - - yes Israel Bedouin - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) - likely pathogenic g.99012747C>T g.98396284C>T c.1114C>T I c.1114C>T - CNGA3_000036 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0294-4 PubMed: Zelinger 2015 - - yes Israel Bedouin - - - - 1 LOVD
+?/. - c.1114C>T r.(?) p.(Pro372Ser) - Parent #1 - likely pathogenic g.99012747C>T g.98396284C>T c.1114C>T I c.1981C>A - CNGA3_000036 heterozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease CHRD2786 PubMed: Zelinger 2015 - - no United States Spanish - - - - 1 LOVD
+?/. p.(Pro372Ser) c.1114C>T r.(?) p.(Pro372Ser) - Parent #2 - likely pathogenic g.99012747C>T g.98396284C>T CNGA3 1114C>T, Pro372Ser - CNGA3_000036 heterozygous PubMed: Georgiou 2019 - - Unknown ? - - - - DNA ? - retrospective research retinal disease KS_10337 PubMed: Georgiou 2019 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Both (homozygous) ACMG pathogenic g.99012747C>T g.98396284C>T CNGA3 c.1114C>T - CNGA3_000036 homozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 7 ; number of affected individuals: 8; segregation analysis: both parents: 5, one parent or other relatives: 2; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Parent #1 ACMG pathogenic g.99012747C>T g.98396284C>T CNGA3 c.1114C>T - CNGA3_000036 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 3 ; number of affected individuals: 4; segregation analysis: both parents: 2, one parent or other relatives: 1; no segregation analysis possible: 1 - - - - - - - - 1 LOVD
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Parent #1 ACMG pathogenic g.99012747C>T g.98396284C>T CNGA3 c.1114C>T - CNGA3_000036 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.1114C>T r.(?) p.(Pro372Ser) - Parent #1 ACMG pathogenic g.99012747C>T g.98396284C>T CNGA3 c.1114C>T - CNGA3_000036 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.1114C>T r.(?) p.(Pro372Ser) - Parent #2 ACMG pathogenic g.99012747C>T g.98396284C>T CNGA3 c.1114C>T - CNGA3_000036 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
+/. - c.1114C>T r.(?) p.(Pro372Ser) - Parent #2 ACMG pathogenic g.99012747C>T g.98396284C>T CNGA3 c.1114C>T - CNGA3_000036 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - 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
Legend   How to query  


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