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TP53 c.277_278insCCTGGCCCCT ;(p.L93Pfs*59)
Variant ID: 17-7579409-A-AAGGGGCCAGG
NM_000546.5(
TP53
):c.277_278insCCTGGCCCCT;(p.L93Pfs*59)
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:
Mutation allele frequency threshold does not affect prognostic analysis using next-generation sequencing in oral squamous cell carcinoma.
Bmc Cancer
Ma, Jie J; Fu, Yong Y; Tu, Yao-Yao YY; Liu, Ying Y; Tan, Yi-Ran YR; Ju, Wu-Tong WT; Pickering, Curtis R CR; Myers, Jeffrey N JN; Zhang, Zhi-Yuan ZY; Zhong, Lai-Ping LP
Publication Date: 2018-07-24
Variant appearance in text: N/A
PubMed Link:
30041611
Variant Present in the following documents:
View BVdb publication page
NRAS germline variant G138R and multiple rare somatic mutations on APC in colorectal cancer patients in Taiwan by next generation sequencing.
Oncotarget
Chang, Pi-Yueh PY; Chen, Jinn-Shiun JS; Chang, Nai-Chung NC; Chang, Shih-Cheng SC; Wang, Mei-Chia MC; Tsai, Shu-Hui SH; Wen, Ying-Hao YH; Tsai, Wen-Sy WS; Chan, Err-Cheng EC; Lu, Jang-Jih JJ
Publication Date: 2016-06-21
Variant appearance in text: TP53: 277_278insCCTGGCCCCT
PubMed Link:
27121310
Variant Present in the following documents:
Main text
oncotarget-07-37566.pdf
View BVdb publication page