Variant #0000338322 (NC_000015.9:g.49083577C>T, NC_000015.9(NM_014985.3):c.833-4G>A (CEP152))

Chromosome 15
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.49083577C>T
DNA change (hg38) g.48791380C>T
Published as CEP152(NM_001194998.1):c.833-4G>A, CEP152(NM_001194998.2):c.833-4G>A
ISCN -
DB-ID CEP152_000049 See all 3 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) 0.39859 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.833-4G>A r.spl? p.?
CEP152 NM_014985.3 -/. - c.833-4G>A r.spl? p.?


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