Variant #0000537828 (NC_000009.11:g.21994259C>A, NM_000077.4:c.-19433G>T (CDKN2A))

Chromosome 9
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.21994259C>A
DNA change (hg38) g.21994260C>A
Published as CDKN2A(NM_058195.3):c.72G>T (p.V24=)
ISCN -
DB-ID CDKN2A_000189
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 12:47:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 -?/. - c.-19433G>T r.(?) p.(=)
CDKN2B NM_004936.3 -?/. - c.*11727G>T r.(=) p.(=)
CDKN2A NM_058195.3 -?/. - c.72G>T r.(?) p.(Val24=)


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