View genomic variant #0000006996

Individual ID 00001252
Chromosome 17
Allele Unknown
Affects function (reported) Does not affect function
Affects function (concluded) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.7676154G>C
Reference -
DB-ID TP53_000001 See all 37 reported entries
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 -/- 4 c.215C>G r.(?) p.(Pro72Arg) Hetero no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001491 DNA SEQ-NG Domeq&Lafage - 27-sep-2019 Multigenetic panel BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, PMS2, PTEN, SMAD4, STK11, TP53 16 Lina Nuñez-Private Practice