Variant #0000000764 (NC_000017.11:g.7673822T>G, NM_000546.5:c.798A>C (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.7673822T>G
Published as G266G
Reference A A Yusoff et al. (2004)
DB-ID TP53_000037 See all 2 reported entries
dbSNP ID rs756044708
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 14:59:14 +08:00 (CST)
Date last edited 2021-09-12 10:40:14 +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.798A>C - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

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