Variant #0000000053 (NC_000002.11:g.99012481G>A, CNGA3(NM_001298.2):c.848G>A)

Individual ID 00000072
Chromosome 2
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.99012481G>A
Reference -
DB-ID CNGA3_000001
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
CNGA3 NM_001298.2 +/+ - c.848G>A r.(?) p.(Arg283Gln) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000072 DNA SEQ-NG CNGA3 1 variome.ir