Variant #0000861607 (NC_000009.11:g.21971122_21971140del, NM_000077.4:c.225_243del (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.21971122_21971140del
DNA change (hg38) -
Published as CDKN2A(NM_000077.4):c.225_243del (p.(Ala76Cysfs*64)), CDKN2A(NM_000077.4):c.225_243delCGCCACTCTCACCCGACCC (p.Ala76Cysfs*64), CDKN2A(NM_001195132.1)...
ISCN -
DB-ID CDKN2A_000079 See all 16 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 +/. - c.225_243del r.(?) p.(Ala76CysfsTer64)
CDKN2A NM_058195.3 +/. - c.268_286del r.(?) p.(Arg90ValfsTer76)


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