Variant #0000000770 (NC_000017.11:g.7674893C>G, NM_000546.5:c.638G>C (TP53))

Individual ID 00000150
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.7674893C>G
Published as R213P
Reference A A Yusoff et al. (2004), dbSNP, ClinVar
DB-ID TP53_000043
dbSNP ID rs587778720
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 16:15:57 +08:00 (CST)
Date last edited 2021-08-23 10:04:52 +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 ./. 6 c.638G>C - r.(?) p.(Arg213Pro) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

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