Variant #0000971889 (NC_000002.11:g.99012444C>A, NM_001298.2:c.811C>A (CNGA3))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.99012444C>A
DNA change (hg38) g.98395981C>A
Published as -
ISCN -
DB-ID CNGA3_000271 See all 3 reported entries
Variant remarks in vitro functional analysis normalized overall luminescence signal (AUC) 0.03±0.01
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) 0 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CNGA3 NM_001298.2 +/. - c.811C>A - p.Pro271Thr TM3 - TM4


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