TNFRSF11A c.989T>C ;(p.V330A)

Variant ID: 18-60036139-T-C

NM_003839.3(TNFRSF11A):c.989T>C;(p.V330A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Bone fragility in patients affected by congenital diseases non skeletal in origin.

Orphanet Journal Of Rare Diseases
Masi, L L; Ferrari, S S; Javaid, M K MK; Papapoulos, S S; Pierroz, D D DD; Brandi, M L ML; ,
Publication Date: 2021-01-06

Variant appearance in text: RANK: 989T>C
PubMed Link: 33407701
Variant Present in the following documents:
  • 13023_2020_Article_1611.pdf
View BVdb publication page



The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine.

Genome Medicine
Garofalo, Andrea A; Sholl, Lynette L; Reardon, Brendan B; Taylor-Weiner, Amaro A; Amin-Mansour, Ali A; Miao, Diana D; Liu, David D; Oliver, Nelly N; MacConaill, Laura L; Ducar, Matthew M; Rojas-Rudilla, Vanesa V; Giannakis, Marios M; Ghazani, Arezou A; Gray, Stacy S; Janne, Pasi P; Garber, Judy J; Joffe, Steve S; Lindeman, Neal N; Wagle, Nikhil N; Garraway, Levi A LA; Van Allen, Eliezer M EM
Publication Date: 2016-07-26

Variant appearance in text: TNFRSF11A: 989T>C; V330A
PubMed Link: 27460824
Variant Present in the following documents:
  • 13073_2016_333_MOESM4_ESM.xlsx, sheet 1
  • 13073_2016_333_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page