View genomic variant #0000006101

Individual ID 00000893
Chromosome 17
Allele Unknown
Affects function (reported) Probably affects function
Affects function (concluded) Probably affects function
DNA change (genomic) (Relative to hg38 / GRCh38) g.7670699C>G
Reference -
DB-ID TP53_000012
Average frequency (large NGS studies) Variant not found in online data sets
Owner Jesica Ramirez-Hospital Central de Mendoza




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Reference     
TP53 NM_000546.5 +?/+? 10 c.1010G>C r.(?) p.(Arg337Pro) Hetero N/A -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001063 DNA CNVs;SEQ-NG Color-Genda Hereditary Cancer Risk Test (30 genes) 20-dec-2018 Multigenetic panel - 1 Jesica Ramirez-Hospital Central de Mendoza