View genomic variant #0000003662

Individual ID 00000459
Chromosome 17
Allele Unknown
Affects function (reported) Effect unknown
Affects function (concluded) Probably does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.7673183G>A
Reference Reclassified June 2019
DB-ID TP53_000010
Average frequency (large NGS studies) Variant not found in online data sets
Owner Pablo Kalfayan-CEMIC




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Reference     
TP53 NM_000546.5 ?/-? 9i c.993+352C>T r.(=) p.(=) Hetero no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000516 DNA SEQ-NG CEMIC - 12-jul-2017 - TP53 4 Pablo Kalfayan-CEMIC