Variant #0000549368 (NC_000012.11:g.88487688dup, NM_025114.3:c.3175dup (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.88487688dup
DNA change (hg38) g.88093911dup
Published as CEP290(NM_025114.3):c.3175dupA (p.I1059Nfs*11), CEP290(NM_025114.4):c.3175dupA (p.I1059Nfs*11)
ISCN -
DB-ID CEP290_000055 See all 18 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.*45489dup r.(?) p.(=)
CEP290 NM_025114.3 +/. - c.3175dup r.(?) p.(Ile1059AsnfsTer11)


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