Variant #0000889624 (NC_000011.9:g.117252488dup, NM_014956.4:c.1481dup (CEP164))

Chromosome 11
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.117252488dup
DNA change (hg38) -
Published as CEP164(NM_014956.4):c.1481dupC (p.P495Sfs*43), CEP164(NM_014956.5):c.1481dupC (p.P495Sfs*43)
ISCN -
DB-ID CEP164_000061 See all 2 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP164 NM_014956.4 ?/. - c.1481dup r.(?) p.(Pro495SerfsTer43)


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