Variant #0000269976 (NC_000012.11:g.88535167T>G, NC_000012.11(NM_025114.3):c.-27-56A>C (CEP290))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88535167T>G
DNA change (hg38) g.88141390T>G
Published as CEP290(NM_025114.4):c.-27-56A>C
ISCN -
DB-ID CEP290_000251
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*92968T>G r.(=) p.(=)
CEP290 NM_025114.3 -/. - c.-27-56A>C r.(=) p.(=)
TMTC3 NM_181783.3 -/. - c.-1126T>G r.(?) p.(=)


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