Variant #0000000039 (NC_000016.9:g.57998033C>T, CNGB1(NM_001297.4):c.290+1G>A)

Individual ID 00000054
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.57998033C>T
Reference -
DB-ID CNGB1_000002
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
CNGB1 NM_001297.4 +/+ - c.290+1G>A r.spl? p.? Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000054 DNA SEQ-NG CNGB1 1 variome.ir