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HR c.1186G>C ;(p.G396R)
Variant ID: 8-21984769-C-G
NM_005144.4(
HR
):c.1186G>C;(p.G396R)
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:
An Asia-specific variant of human IgG1 represses colorectal tumorigenesis by shaping the tumor microenvironment.
The Journal Of Clinical Investigation
Yang, Bing B; Zhang, Zhen Z; Chen, Xiangjun X; Wang, Xu-Yan XY; Qin, Shishang S; Du, Liaoqi L; Yang, Changjiang C; Zhu, Liyu L; Sun, Wenbo W; Zhu, Yongjie Y; Zheng, Qinwen Q; Zhao, Shidong S; Wang, Quan Q; Zhao, Long L; Lin, Yilin Y; Huang, Jinghe J; Wu, Fan F; Lu, Lu L; Wang, Fei F; Zheng, Wenjie W; Zhou, Xiao-Hua XH; Zhao, Xiaozhen X; Wang, Ziye Z; Xiao-Lin, Sun S; Ye, Yingjiang Y; Wang, Shan S; Li, Zhanguo Z; Qi, Hai H; Zhang, Zemin Z; Kuang, Dong-Ming DM; Zhang, Lei L; Shen, Zhanlong Z; Liu, Wanli W
Publication Date: 2022-03-15
Variant appearance in text: HR: G396R
PubMed Link:
35133976
Variant Present in the following documents:
jci-132-153454-s129.pdf
View BVdb publication page