Variant #0000268082 (NC_000006.11:g.36652129G>A, NM_078467.2:c.251G>A (CDKN1A))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36652129G>A
DNA change (hg38) g.36684352G>A
Published as CDKN1A(NM_001220778.2):c.251G>A (p.R84Q), CDKN1A(NM_001291549.1):c.353G>A (p.R118Q), CDKN1A(NM_001291549.3):c.353G>A (p.R118Q)
ISCN -
DB-ID CDKN1A_000005 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) 0.00247 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN1A NM_078467.2 -?/. - c.251G>A r.(?) p.(Arg84Gln)


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