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.

9 entries on 1 page. Showing entries 1 - 9.
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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.513G>T r.(?) p.(Trp171Cys) - Unknown - VUS g.99006184G>T g.98389721G>T - - CNGA3_000061 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.513G>T r.(?) p.(Trp171Cys) - Parent #1 - likely pathogenic (recessive) g.99006184G>T g.98389721G>T - - CNGA3_000061 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT660 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.513G>T r.(?) p.(Trp171Cys) - Parent #1 - likely pathogenic (recessive) g.99006184G>T g.98389721G>T - - CNGA3_000061 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT1071 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.513G>T r.(?) p.(Trp171Cys) - Parent #2 - likely pathogenic g.99006184G>T g.98389721G>T CNGA3 c.[464del];[513G>T] - CNGA3_000061 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 15890 PubMed: Sun 2020 - F - China - - - - - 1 LOVD
+?/. - c.513G>T r.(?) p.(Trp171Cys) - Parent #1 - likely pathogenic g.99006184G>T g.98389721G>T CNGA3 c.[513G>T];[633T>A] - CNGA3_000061 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 11802 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. - c.513G>T r.(?) p.(Trp171Cys) - Unknown - likely pathogenic g.99006184G>T g.98389721G>T CNGA3 c.513G>T(;)1627_1635del - CNGA3_000061 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 14792 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. - c.513G>T r.(?) p.(Trp171Cys) - Parent #1 - likely pathogenic g.99006184G>T g.98389721G>T CNGA3 c.513G>T, p.W171C - CNGA3_000061 heterozygous PubMed: Liang 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease F4-II1 PubMed: Liang 2015 - M - China - - - - - 1 LOVD
+?/. - c.513G>T r.(?) p.(Trp171Cys) TM1 Unknown - likely pathogenic (recessive) g.99006184G>T g.98389721G>T - - CNGA3_000061 ACMG PM2_mod, PM1_sup, PP2_sup, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.513G>T - p.Trp171Cys TM1 Unknown - NA g.99006184G>T g.98389721G>T - - CNGA3_000061 in vitro functional analysis normalized overall luminescence signal (AUC) 0.16±0.06, normalized peak latency 2.98±0.13 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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