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.

19 entries on 1 page. Showing entries 1 - 19.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 7 c.985G>T r.(?) p.(Gly329Cys) - Both (homozygous) - likely pathogenic g.99012618G>T g.98396155G>T - - CNGA3_000051 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - M yes Israel Arab-Muslim - - - - 3 Dror Sharon
+?/. 7 c.985G>T r.(?) p.(Gly329Cys) - Paternal (confirmed) - likely pathogenic g.99012618G>T g.98396155G>T - - CNGA3_000051 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - M no Israel Jewish-Ashkenazi - - - - 1 Dror Sharon
+?/. 7 c.985G>T r.(?) p.(Gly329Cys) - Paternal (confirmed) - likely pathogenic g.99012618G>T g.98396155G>T - - CNGA3_000051 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - M no Israel Arab-Muslim - - - - 1 Dror Sharon
+?/. 7 c.985G>T r.(?) p.(Gly329Cys) - Maternal (confirmed) - likely pathogenic g.99012618G>T g.98396155G>T - - CNGA3_000051 - Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - M no Israel Arab-Muslim - - - - 2 Dror Sharon
+/. - c.985G>T r.(?) p.(Gly329Cys) - Unknown ACMG pathogenic g.99012618G>T - - - CNGA3_000051 - PubMed: Sharon 2019 - - Germline - 4/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 4 IRD families - - Israel - - - - - 4 Global Variome, with Curator vacancy
+/. - c.985G>T r.(?) p.(Gly329Cys) - Unknown ACMG pathogenic g.99012618G>T - - - CNGA3_000051 - 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
+?/. 7 c.985G>T r.(?) p.(Gly329Cys) - Parent #1 - likely pathogenic g.99012618G>T g.98396155G>T allele 1: c.985G>T - p.Gly329Cys, allele 2: c.1306C>T - p.Arg436Trp - CNGA3_000051 heterozygous PubMed: Genead 2011 - - Unknown ? - - - - DNA SEQ blood - retinal disease 6 PubMed: Genead 2011 - F - United States Jordanian - - - - 1 LOVD
+?/. 7 c.985G>T r.(?) p.(Gly329Cys) - Parent #1 - likely pathogenic g.99012618G>T g.98396155G>T allele 1: c.985G>T - p.Gly329Cys, allele 2: c.1306C>T - p.Arg436Trp - CNGA3_000051 heterozygous PubMed: Genead 2011 - - Unknown ? - - - - DNA SEQ blood - retinal disease 12 PubMed: Genead 2011 - M - United States Jordanian - - - - 1 LOVD
+?/. - c.985G>T r.(?) p.(Gly329Cys) - Parent #1 - likely pathogenic g.99012618G>T g.98396155G>T c.985G>T I c.811C>G - CNGA3_000051 heterozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0238-2 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.985G>T r.(?) p.(Gly329Cys) - Both (homozygous) - likely pathogenic g.99012618G>T g.98396155G>T c.985G>T I c.985G>T - CNGA3_000051 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0476-1 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.985G>T r.(?) p.(Gly329Cys) - Both (homozygous) - likely pathogenic g.99012618G>T g.98396155G>T c.985G>T I c.985G>T - CNGA3_000051 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0476-5 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.985G>T r.(?) p.(Gly329Cys) - Parent #2 - likely pathogenic g.99012618G>T g.98396155G>T c.829C>T I c.985G>T - CNGA3_000051 heterozygous PubMed: Zelinger 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0216-1 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. p.(Gly329Cys) c.985G>T r.(?) p.(Gly329Cys) - Both (homozygous) - likely pathogenic g.99012618G>T g.98396155G>T CNGA3 985G>T, Gly329Cys - CNGA3_000051 homozygous PubMed: Georgiou 2019 - - Unknown ? - - - - DNA ? - retrospective research retinal disease JC_0674 PubMed: Georgiou 2019 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.985G>T r.(?) p.(Gly329Cys) - Parent #1 ACMG pathogenic g.99012618G>T g.98396155G>T - - CNGA3_000051 - PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - - Germline - - - - - DNA MIPsm - smMIPs 105 iMD/AMD genes retinal disease 070748 PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 presumed digenic inheriance with CNGB3 variant M - - - - - - - 1 Rebekkah Hitti-Malin
+/. - c.985G>T r.(?) p.(Gly329Cys) - Parent #2 ACMG pathogenic g.99012618G>T g.98396155G>T - - CNGA3_000051 - PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - - Germline - - - - - DNA MIPsm - smMIPs 105 iMD/AMD genes retinal disease 070241 PubMed: Hitti-Malin 2022, Journal: Hitti-Malin 2022 - F - - - - - - - 1 Rebekkah Hitti-Malin
+/. - c.985G>T r.(?) p.(Gly329Cys) - Both (homozygous) ACMG pathogenic g.99012618G>T g.98396155G>T CNGA3 c.985G>T - CNGA3_000051 homozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 6; segregation analysis: both parents: 6, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.985G>T r.(?) p.(Gly329Cys) - Unknown ACMG pathogenic (recessive) g.99012618G>T g.98396155G>T - - CNGA3_000051 ACMG PP3, PM2, PM1, PP2, PP5_STRONG PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? ACHM-1271 PubMed: Weisschuh 2024 family, 2 affected F - Germany - - - - - 2 Johan den Dunnen
+/. - c.985G>T r.(?) p.(Gly329Cys) TM5 - pore helix Unknown - pathogenic (recessive) g.99012618G>T g.98396155G>T - - CNGA3_000051 ACMG PP1_sup, PP5_strong, PM1_mod, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.985G>T - p.Gly329Cys TM5 - pore helix Unknown - NA g.99012618G>T g.98396155G>T - - CNGA3_000051 in vitro functional analysis normalized overall luminescence signal (AUC) 0.02±0.00 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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