Variant #0000852231 (NC_000009.11:g.22008739G>A, NC_000009.11(NM_004936.3):c.156+58C>T (CDKN2B))

Chromosome 9
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.22008739G>A
DNA change (hg38) -
Published as CDKN2B(NM_078487.2):c.214C>T (p.R72W)
ISCN -
DB-ID CDKN2B_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2B NM_004936.3 ?/. - c.156+58C>T r.(=) p.(=)
CDKN2B-AS1 NR_003529.3 ?/. - n.371+13579G>A r.(?) -


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