TP53 c.658_660del ;(p.Y220del)

Variant ID: 17-7578189-CATA-C

NM_000546.5(TP53):c.658_660del;(p.Y220del)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genetic and functional analysis of a Li Fraumeni syndrome family in China.

Scientific Reports
Hu, Huaying H; Liu, Jingping J; Liao, Xinbin X; Zhang, Shuju S; Li, Haibo H; Lu, Renbin R; Li, Xianfeng X; Lin, Wei W; Liu, Minji M; Xia, Zanxian Z; Qing, Guoliang G; Li, Jia-Da JD
Publication Date: 2016-01-28

Variant appearance in text: TP53: Y220del
PubMed Link: 26818906
Variant Present in the following documents:
  • Main text
  • srep20221.pdf
View BVdb publication page