Variant #0000528779 (NC_000006.11:g.36652228G>A, NM_078467.2:c.350G>A (CDKN1A))

Chromosome 6
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.36652228G>A
DNA change (hg38) g.36684451G>A
Published as CDKN1A(NM_000389.4):c.350G>A (p.(Cys117Tyr)), CDKN1A(NM_001291549.1):c.452G>A (p.C151Y), CDKN1A(NM_001291549.3):c.452G>A (p.C151Y), CDKN1A(NM_0784...)
ISCN -
DB-ID CDKN1A_000007 See all 5 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) 0.0019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN1A NM_078467.2 ?/. - c.350G>A r.(?) p.(Cys117Tyr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.