Variant #0001062695 (NC_000012.11:g.12870938G>A, NM_004064.3:c.165G>A (CDKN1B))

Chromosome 12
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.12870938G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDKN1B_000031
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs16908375
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00305 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-01-09 10:35:01 +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     
CDKN1B NM_004064.3 -/. - c.165G>A r.(?) p.(Ala55=)


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