EBV Mutation Detail Information

> G162852T Search Result

Mutation Information

Mutation Site	G162852T
Mutation Type	Nucleotide level
Gene/Protein/Region Type	BALF2
Viral Reference	NC007605.1
Country	Guangzhou;China

Literature Information

PubMed PMID	31209392
Disease	Nasopharyngeal carcinoma; Burkitt lymphoma; Hodgkin lymphoma; NK/T cell lymphoma; Gastric carcinoma
Published Year	2019
Journal	Nature genetics
Title	Genome sequencing analysis identifies Epstein-Barr virus subtypes associated with high risk of nasopharyngeal carcinoma.
Author	Xu M,Yao Y,Chen H,Zhang S,Cao SM,Zhang Z,Luo B,Liu Z,Li Z,Xiang T,He G,Feng QS,Chen LZ,Guo X,Jia WH,Chen MY,Zhang X,Xie SH,Peng R,Chang ET,Pedergnana V,Feng L,Bei JX,Xu RH,Zeng MS,Ye W,Adami HO,Lin X,Zhai W,Zeng YX,Liu J
Evidence	The red line is the suggestive genome-wide significance P value threshold of 4.07×10−4. The three SNPs 162507C>T, 162852G>T and 162215C>A reaching genome-wide significance are labeled as green.

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Description

Mutation Information Note

Gene/Protein/Region Type: Virus Gene (e.g. LMP-1) or Virus Protein (e.g. Rep 68) or Virus Region (e.g. S, X)

Literature Information Note

Evidence: sentence contains this mutation information in the citation