Bibliome.ai browser hg19
Search
About
Stats
FAQ
TNFSF11 c.81G>A ;(p.E27=)
Variant ID: 13-43148520-G-A
NM_003701.3(
TNFSF11
):c.81G>A;(p.E27=)
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:
Lack of Myosin X Enhances Osteoclastogenesis and Increases Cell Surface Unc5b in Osteoclast-Lineage Cells.
Journal Of Bone And Mineral Research : The Official Journal Of The American Society For Bone And Mineral Research
Wang, Bo B; Pan, Jin-Xiu JX; Yu, Huali H; Xiong, Lei L; Zhao, Kai K; Xiong, Shan S; Guo, Jun-Peng JP; Lin, Sen S; Sun, Dong D; Zhao, Lu L; Guo, Haohan H; Mei, Lin L; Xiong, Wen-Cheng WC
Publication Date: 2019-05
Variant appearance in text: RANKL: E27E
PubMed Link:
30645777
Variant Present in the following documents:
Main text
View BVdb publication page