GPNMB c.389C>T ;(p.P130L)

Variant ID: 7-23296532-C-T

NM_002510.2(GPNMB):c.389C>T;(p.P130L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Intra-tumor genetic heterogeneity and alternative driver genetic alterations in breast cancers with heterogeneous HER2 gene amplification.

Genome Biology
Ng, Charlotte K Y CK; Martelotto, Luciano G LG; Gauthier, Arnaud A; Wen, Huei-Chi HC; Piscuoglio, Salvatore S; Lim, Raymond S RS; Cowell, Catherine F CF; Wilkerson, Paul M PM; Wai, Patty P; Rodrigues, Daniel N DN; Arnould, Laurent L; Geyer, Felipe C FC; Bromberg, Silvio E SE; Lacroix-Triki, Magali M; Penault-Llorca, Frederique F; Giard, Sylvia S; Sastre-Garau, Xavier X; Natrajan, Rachael R; Norton, Larry L; Cottu, Paul H PH; Weigelt, Britta B; Vincent-Salomon, Anne A; Reis-Filho, Jorge S JS
Publication Date: 2015-05-22

Variant appearance in text: GPNMB: P130L
PubMed Link: 25994018
Variant Present in the following documents:
  • 13059_2015_657_MOESM9_ESM.pdf
View BVdb publication page