Variant #0000324097 (NC_000015.9:g.49054632C>T, NM_014985.3:c.2518G>A (CEP152))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49054632C>T
DNA change (hg38) g.48762435C>T
Published as CEP152(NM_001194998.1):c.2518G>A (p.(Glu840Lys))
ISCN -
DB-ID CEP152_000034
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) 0.00104 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.2518G>A r.(?) p.(Glu840Lys)
CEP152 NM_014985.3 ?/. - c.2518G>A r.(?) p.(Glu840Lys)


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