Variant #0000888791 (NC_000009.11:g.22006147C>T, NM_004936.3:c.256G>A (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.22006147C>T
DNA change (hg38) -
Published as CDKN2B(NM_004936.4):c.256G>A (p.D86N)
ISCN -
DB-ID CDKN2B_000001 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) 0.00122 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.256G>A r.(?) p.(Asp86Asn)
CDKN2B-AS1 NR_003529.3 ?/. - n.371+10987C>T r.(?) -


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