Variant #0000971843 (NC_000002.11:g.98986506G>A, NM_001298.2:c.68G>A (CNGA3))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.98986506G>A
DNA change (hg38) g.98370043G>A
Published as -
ISCN -
DB-ID CNGA3_000309 See all 2 reported entries
Variant remarks in vitro functional analysis normalized overall luminescence signal (AUC) 0.81±0.05, normalized peak latency 0.89±0.03
Reference PubMed: Solaki 2023
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-03-13 10:38:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CNGA3 NM_001298.2 -/. - c.68G>A - p.Arg23Gln N-Term


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