Variant #0000554725 (NC_000015.9:g.49059531C>T, NC_000015.9(NM_014985.3):c.2147+1G>A (CEP152))

Chromosome 15
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.49059531C>T
DNA change (hg38) g.48767334C>T
Published as CEP152(NM_001194998.2):c.2147+1G>A
ISCN -
DB-ID CEP152_000075
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP152 NM_001194998.1 +/. - c.2147+1G>A r.spl? p.?
CEP152 NM_014985.3 +/. - c.2147+1G>A r.spl? p.?


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