Variant #0000614418 (NC_000012.11:g.88534780_88534783del, NM_025114.3:c.133_136del (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.88534780_88534783del
DNA change (hg38) g.88141003_88141006del
Published as CEP290(NM_025114.4):c.133_136delCAAG (p.Q45Kfs*3)
ISCN -
DB-ID CEP290_000387
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +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.*92581_*92584del r.(=) p.(=)
CEP290 NM_025114.3 +/. - c.133_136del r.(?) p.(Gln45LysfsTer3)
TMTC3 NM_181783.3 +/. - c.-1513_-1510del r.(?) p.(=)


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