Variant #0000888790 (NC_000009.11:g.21974769C>A, NM_000077.4:c.58G>T (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.21974769C>A
DNA change (hg38) -
Published as CDKN2A(NM_000077.5):c.58G>T (p.A20S)
ISCN -
DB-ID CDKN2A_000188 See all 2 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) 0 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 ?/. - c.58G>T r.(?) p.(Ala20Ser)
CDKN2A NM_058195.3 ?/. - c.194-3562G>T r.(=) p.(=)


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