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TP53 c.1171del ;(p.D391Tfs*31)
Variant ID: 17-7572938-TC-T
NM_000546.5(
TP53
):c.1171del;(p.D391Tfs*31)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis.
Nature Genetics
Kar, Siddhartha P SP; Quiros, Pedro M PM; Gu, Muxin M; Jiang, Tao T; Mitchell, Jonathan J; Langdon, Ryan R; Iyer, Vivek V; Barcena, Clea C; Vijayabaskar, M S MS; Fabre, Margarete A MA; Carter, Paul P; Petrovski, Slavé S; Burgess, Stephen S; Vassiliou, George S GS
Publication Date: 2022-08
Variant appearance in text: TP53: D391Tfs*31
PubMed Link:
35835912
Variant Present in the following documents:
41588_2022_1121_MOESM3_ESM.xlsx, sheet 4
View BVdb publication page
Cancer-derived C-terminus-extended p53 mutation confers dominant-negative effect on its wild-type counterpart.
Journal Of Molecular Cell Biology
Huang, Shibo S; Cao, Bo B; Wang, Jieqiong J; Zhang, Yiwei Y; Ledet, Elisa E; Sartor, Oliver O; Xiong, Yuqin Y; Zeng, Shelya X SX; Lu, Hua H
Publication Date: 2022-03-29
Variant appearance in text: p53: D391Tfs*31
PubMed Link:
34918105
Variant Present in the following documents:
mjab078_supplemental_file.pdf
View BVdb publication page