NF1 c.1138C>T ;(p.L380F)

Variant ID: 17-29528130-C-T

NM_001042492.2(NF1):c.1138C>T;(p.L380F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Assessment of Minimal Residual Disease by Next Generation Sequencing in Peripheral Blood as a Complementary Tool for Personalized Transplant Monitoring in Myeloid Neoplasms.

Journal Of Clinical Medicine
Aguirre-Ruiz, Paula P; Ariceta, Beñat B; Viguria, María Cruz MC; Zudaire, María Teresa MT; Blasco-Iturri, Zuriñe Z; Arnedo, Patricia P; Aguilera-Diaz, Almudena A; Jauregui, Axier A; Mañú, Amagoia A; Prosper, Felipe F; Mateos, María Carmen MC; Fernández-Mercado, Marta M; Larráyoz, María José MJ; Redondo, Margarita M; Calasanz, María José MJ; Vázquez, Iria I; Bandrés, Eva E
Publication Date: 2020-11-25

Variant appearance in text: NF1: 1138C>T; Leu380Phe
PubMed Link: 33255857
Variant Present in the following documents:
  • Main text
  • jcm-09-03818.pdf
View BVdb publication page



Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas.

Cell Reports
Way, Gregory P GP; Sanchez-Vega, Francisco F; La, Konnor K; Armenia, Joshua J; Chatila, Walid K WK; Luna, Augustin A; Sander, Chris C; Cherniack, Andrew D AD; Mina, Marco M; Ciriello, Giovanni G; Schultz, Nikolaus N; , ; Sanchez, Yolanda Y; Greene, Casey S CS
Publication Date: 2018-04-03

Variant appearance in text: NF1: 1138C>T
PubMed Link: 29617658
Variant Present in the following documents:
  • NIHMS958974-supplement-5.xlsx, sheet 1
View BVdb publication page