Variant #0000003026 (NC_000017.11:g.12139G>C, NM_000546.5:c.*7657470C>G (TP53))

Individual ID 00000762
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.12139G>C
Published as -
Reference A R Ghani et al.(2008)
DB-ID TP53_000060
dbSNP ID -
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-07-06 13:02:01 +08:00 (CST)
Date last edited 2021-08-01 13:21:44 +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 +/. 4 c.*7657470C>G - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000856 DNA PCR;SEQ TP53 1 Nur Aisyah Athirah