Bibliome.ai browser hg19
Search
About
Stats
FAQ
TP53 c.919+1dup
Variant ID: 17-7577017-A-AC
NM_000546.5(
TP53
):c.919+1dup
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:
Characteristics of Li-Fraumeni Syndrome in Japan; A Review Study by the Special Committee of JSHT.
Cancer Science
Funato, Michinori M; Tsunematsu, Yukiko Y; Yamazaki, Fumito F; Tamura, Chieko C; Kumamoto, Tadashi T; Takagi, Masatoshi M; Kato, Shunsuke S; Sugimura, Haruhiko H; Tamura, Kazuo K
Publication Date: 2021-05-01
Variant appearance in text: TP53: 918_919insG
PubMed Link:
33932062
Variant Present in the following documents:
Main text
View BVdb publication page