Variant #0000724273 (NC_000012.11:g.88483027G>A, NM_025114.3:c.3811C>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.88483027G>A
DNA change (hg38) -
Published as CEP290(NM_025114.4):c.3811C>T (p.R1271*)
ISCN -
DB-ID CEP290_000058 See all 14 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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf29 NM_001009894.2 +/. - c.*40828G>A r.(=) p.(=)
CEP290 NM_025114.3 +/. - c.3811C>T r.(?) p.(Arg1271Ter)


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