Variant #0000887878 (NC_000007.13:g.39990724dup, NM_003718.4:c.484dup (CDK13))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39990724dup
DNA change (hg38) -
Published as CDK13(NM_003718.5):c.484dup (p.(Ala162GlyfsTer108)), CDK13(NM_003718.5):c.484dupG (p.A162Gfs*108)
ISCN -
DB-ID CDK13_000038 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK13 NM_003718.4 +?/. - c.484dup r.(?) p.(Ala162Glyfs*108)


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