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.




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