View genomic variant #0000005664

Individual ID 00000786
Chromosome 17
Allele Unknown
Affects function (reported) Effect unknown
Affects function (concluded) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.7674187T>C
Reference -
DB-ID TP53_000011
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lina Nuñez-Private Practice




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Reference     
TP53 NM_000546.5 ?/? 7 c.776A>G r.(?) p.(Asp259Gly) Hetero no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000914 DNA SEQ-NG Color-Genda Hereditary Cancer Risk Test (30 genes) 1-aug-2018 Multigenetic panel - 2 Lina Nuñez-Private Practice