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.

6 entries on 1 page. Showing entries 1 - 6.
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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.553C>G r.(?) p.(Leu185Val) - Parent #1 ACMG VUS g.99006224C>G - - - CNGA3_000085 - PubMed: Kim 2019 - - Germline - 1/86 cases - - - DNA SEQ, SEQ-NG - 204 gene panel retinal disease - PubMed: Kim 2019 - - - Korea - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.553C>G r.(?) p.(Leu185Val) - Unknown ACMG VUS g.99006224C>G - - - CNGA3_000085 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - ACHM IR_GH_0120 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
?/. - c.553C>G r.(?) p.(Leu185Val) - Unknown ACMG VUS g.99006224C>G g.98389761C>G CNGA3 c.553C>G, p.L185V - CNGA3_000085 - PubMed: Kim 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 204 genes associated with inherited retinal disorders, see paper retinal disease ? PubMed: Kim 2019 - ? - Korea, South (Republic) - - - - - 1 LOVD
+?/. - c.553C>G r.(?) p.(Leu185Val) - Maternal (confirmed) - likely pathogenic g.99006224C>G g.98389761C>G - - CNGA3_000085 - PubMed: Moon 2021 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel retinal disease Pat10 PubMed: Moon 2021 - - - Korea - - - - - 1 Johan den Dunnen
-?/. - c.553C>G r.(?) p.(Leu185Val) TM1 Unknown - likely benign g.99006224C>G g.98389761C>G - - CNGA3_000085 ACMG PM2_mod, PM1_sup, PP2_sup, BP4_sup, BS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.553C>G - p.Leu185Val TM1 Unknown - NA g.99006224C>G g.98389761C>G - - CNGA3_000085 in vitro functional analysis normalized overall luminescence signal (AUC) 0.91±0.11, normalized peak latency 0.92±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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