Variant #0000000043 (NC_000016.9:g.57965724G>T, CNGB1(NM_001297.4):c.1431C>A)

Individual ID 00000058
Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.57965724G>T
Reference -
DB-ID CNGB1_000003
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     
CNGB1 NM_001297.4 +/+ - c.1431C>A r.(?) p.(Cys477*) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000058 DNA SEQ-NG CNGB1 1 variome.ir