Variant #0001046197 (NC_000009.11:g.21994178C>A, NM_000077.4:c.-19352G>T (CDKN2A))

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.21994178C>A
DNA change (hg38) -
Published as CDKN2A(NM_058195.4):c.153G>T (p.R51S)
ISCN -
DB-ID CDKN2A_000218
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 ?/. - c.-19352G>T r.(?) p.(=)
CDKN2B NM_004936.3 ?/. - c.*11808G>T r.(=) p.(=)
CDKN2A NM_058195.3 ?/. - c.153G>T r.(?) p.(Arg51Ser)


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