Variant #0001046195 (NC_000009.11:g.21971155G>A, NM_000077.4:c.203C>T (CDKN2A))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21971155G>A
DNA change (hg38) -
Published as CDKN2A(NM_000077.5):c.203C>T (p.A68V)
ISCN -
DB-ID CDKN2A_000074 See all 6 reported entries
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 +?/. - c.203C>T r.(?) p.(Ala68Val)
CDKN2A NM_058195.3 +?/. - c.246C>T r.(?) p.(=)


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