Variant #0000554737 (NC_000015.9:g.49089646C>A, NM_014985.3:c.392G>T (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.49089646C>A
DNA change (hg38) g.48797449C>A
Published as CEP152(NM_001194998.1):c.392G>T (p.(Gly131Val))
ISCN -
DB-ID CEP152_000081
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) 1.0E-5 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 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.392G>T r.(?) p.(Gly131Val)
CEP152 NM_014985.3 ?/. - c.392G>T r.(?) p.(Gly131Val)


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