Variant #0000016608 (NC_000012.11:g.88524101G>A, NM_025114.3:c.613C>T (CEP290))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.88524101G>A
DNA change (hg38) g.88130324G>A
Published as Arg205X
ISCN -
DB-ID CEP290_000020 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs137852835
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-04 16:02:59 +01:00 (CET)
Date last edited 2023-11-27 19:59:42 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP290 NM_025114.3 +/. 9 c.613C>T r.(613c>u) p.(Arg205*)


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