Variant #0000000772 (NC_000017.11:g.7673800_7673803del, NM_000546.5:c.817_820del (TP53))

Individual ID 00000150
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.7673800_7673803del
Published as CTGG, 4 bp-deletion
Reference A A Yusoff et al. (2004)
DB-ID TP53_000045
dbSNP ID rs1564752665
Frequency 1/47
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 2020-11-16 16:32:21 +08:00 (CST)
Date last edited 2021-09-12 10:31:48 +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.817_820del - r.(?) p.(Arg273Phefs*71) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000165 DNA PCR;SSCA TP53 12 Nuur Athirah Binti Mohd Daud