Variant #0000000703 (NC_000017.11:g.7673776G>A, NM_000546.5:c.844C>T (TP53))

Individual ID 00000133
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.7673776G>A
Published as R282W
Reference Sharifah Nurain Syed Zanaruddin et al. (2013), dbSNP, (OMIM 0018), ClinVar
DB-ID TP53_000020 See all 2 reported entries
dbSNP ID rs28934574
Frequency 1/31
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-11-05 11:25:10 +08:00 (CST)
Date last edited 2021-08-22 15:15:02 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
TP53 NM_000546.5 ./. 8 c.844C>T - r.(?) p.(Arg282Trp) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000148 DNA PCR;SEQ TP53 27 Nuur Athirah Binti Mohd Daud