Variant #0001017802 (NC_000009.11:g.21994139T>A, NM_058195.3:c.192A>T (CDKN2A))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21994139T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDKN2A_000209
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1554659172
Origin CLASSIFICATION record
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 2024-11-28 15:54:01 +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     
CDKN2A NM_058195.3 +/. - c.192A>T r.(?) p.(Pro64=)


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