Variant #0001049131 (NC_000012.11:g.12871135C>T, NM_004064.3:c.362C>T (CDKN1B))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.12871135C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDKN1B_000029
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs201685429
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-10 22:50:02 +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     
CDKN1B NM_004064.3 -?/. - c.362C>T r.(?) p.(Ala121Val)


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