Variant #0000269970 (NC_000015.9:g.49088231G>A, NM_014985.3:c.667C>T (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.49088231G>A
DNA change (hg38) g.48796034G>A
Published as CEP152(NM_001194998.1):c.667C>T (p.(Gln223Ter)), CEP152(NM_001194998.2):c.667C>T (p.Q223*)
ISCN -
DB-ID CEP152_000053 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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.667C>T r.(?) p.(Gln223Ter)
CEP152 NM_014985.3 +/. - c.667C>T r.(?) p.(Gln223Ter)


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