Variant #0000000027 (NC_000012.11:g.88479869C>A, CEP290(NM_025114.3):c.4384G>T)

Individual ID 00000033
Chromosome 12
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.88479869C>A
Reference -
DB-ID CEP290_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
CEP290 NM_025114.3 +/+ - c.4384G>T r.(?) p.(Glu1462*) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000034 DNA SEQ-NG CEP290 1 variome.ir