NF1 c.1976G>T ;(p.R659L)

Variant ID: 17-29552243-G-T

NM_001042492.2(NF1):c.1976G>T;(p.R659L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology.

Acta Neuropathologica
Qaddoumi, Ibrahim I; Orisme, Wilda W; Wen, Ji J; Santiago, Teresa T; Gupta, Kirti K; Dalton, James D JD; Tang, Bo B; Haupfear, Kelly K; Punchihewa, Chandanamali C; Easton, John J; Mulder, Heather H; Boggs, Kristy K; Shao, Ying Y; Rusch, Michael M; Becksfort, Jared J; Gupta, Pankaj P; Wang, Shuoguo S; Lee, Ryan P RP; Brat, Daniel D; Peter Collins, V V; Dahiya, Sonika S; George, David D; Konomos, William W; Kurian, Kathreena M KM; McFadden, Kathryn K; Serafini, Luciano Neder LN; Nickols, Hilary H; Perry, Arie A; Shurtleff, Sheila S; Gajjar, Amar A; Boop, Fredrick A FA; Klimo, Paul D PD; Mardis, Elaine R ER; Wilson, Richard K RK; Baker, Suzanne J SJ; Zhang, Jinghui J; Wu, Gang G; Downing, James R JR; Tatevossian, Ruth G RG; Ellison, David W DW
Publication Date: 2016-06

Variant appearance in text: NF1: R659L
PubMed Link: 26810070
Variant Present in the following documents:
  • Main text
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