Variant #0000549347 (NC_000012.11:g.88477732C>A, NC_000012.11(NM_025114.3):c.4705-1G>T (CEP290))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88477732C>A
DNA change (hg38) g.88083955C>A
Published as -
ISCN -
DB-ID CEP290_000009 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 17:18:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf29 NM_001009894.2 +/. - c.*35533C>A r.(=) p.(=)
CEP290 NM_025114.3 +/. - c.4705-1G>T r.spl? p.?


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