Variant #0001049127 (NC_000001.10:g.51435946C>T, NC_000001.10(NM_001262.2):c.-11-84C>T (CDKN2C))

Chromosome 1
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.51435946C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDKN2C_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs41285700
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-10 21:05:01 +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     
CDKN2C NM_001262.2 -/. - c.-11-84C>T r.(?) p.(?)


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