Variant #0000809228 (NC_000020.10:g.34089662_34089663dup, NC_000020.10(NM_007186.3):c.3899-10_3899-9dup (CEP250))

Chromosome 20
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.34089662_34089663dup
DNA change (hg38) -
Published as CEP250(NM_007186.5):c.3902_3903insCT (p.K1301Nfs*12)
ISCN -
DB-ID CEP250_000067
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP250 NM_007186.3 -/. - c.3899-10_3899-9dup r.(=) p.(=)


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