Variant #0000547104 (NC_000012.11:g.12871186_12871187insT, NM_004064.3:c.413_414insT (CDKN1B))

Chromosome 12
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.12871186_12871187insT
DNA change (hg38) g.12718252_12718253insT
Published as CDKN1B(NM_004064.5):c.413_414insT (p.D139Gfs*66)
ISCN -
DB-ID CDKN1B_000013
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN1B NM_004064.3 +/. - c.413_414insT r.(?) p.(Asp139GlyfsTer66)


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