Variant #0000978659 (NC_000009.11:g.21974816G>C, NM_000077.4:c.11C>G (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.21974816G>C
DNA change (hg38) -
Published as CDKN2A(NM_000077.5):c.11C>G (p.A4G)
ISCN -
DB-ID CDKN2A_000207
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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +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.11C>G r.(?) p.(Ala4Gly)
CDKN2A NM_058195.3 ?/. - c.194-3609C>G r.(=) p.(=)


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