Variant #0001029896 (NC_000017.10:g.7577094G>A, NM_000546.5:c.844C>T (TP53))

Chromosome 17
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.7577094G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TP53_010005 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs28934574
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-14 15:21:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 +/. - c.844C>T r.(?) p.(Arg282Trp)


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