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TNFRSF11A c.758C>T ;(p.A253V)
Variant ID: 18-60033968-C-T
NM_003839.3(
TNFRSF11A
):c.758C>T;(p.A253V)
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:
Multi-omics profiling of primary small cell carcinoma of the esophagus reveals RB1 disruption and additional molecular subtypes.
Nature Communications
Li, Renda R; Yang, Zhenlin Z; Shao, Fei F; Cheng, Hong H; Wen, Yaru Y; Sun, Sijin S; Guo, Wei W; Li, Zitong Z; Zhang, Fan F; Xue, Liyan L; Bi, Nan N; Wang, Jie J; Sun, Yingli Y; Li, Yin Y; Tan, Fengwei F; Xue, Qi Q; Gao, Shugeng S; Shi, Susheng S; Gao, Yibo Y; He, Jie J
Publication Date: 2021-06-18
Variant appearance in text: TNFRSF11A: 758C>T; S253L
PubMed Link:
34145257
Variant Present in the following documents:
41467_2021_24043_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
The Genetic Architecture of High Bone Mass.
Frontiers In Endocrinology
Gregson, Celia L CL; Duncan, Emma L EL
Publication Date: 2020
Variant appearance in text: RANK: 758C>T
PubMed Link:
33193107
Variant Present in the following documents:
Main text
View BVdb publication page