NF1 c.226G>C ;(p.E76Q)

Variant ID: 17-29486049-G-C

NM_001042492.2(NF1):c.226G>C;(p.E76Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth.

Jama
Mody, Rajen J RJ; Wu, Yi-Mi YM; Lonigro, Robert J RJ; Cao, Xuhong X; Roychowdhury, Sameek S; Vats, Pankaj P; Frank, Kevin M KM; Prensner, John R JR; Asangani, Irfan I; Palanisamy, Nallasivam N; Dillman, Jonathan R JR; Rabah, Raja M RM; Kunju, Laxmi Priya LP; Everett, Jessica J; Raymond, Victoria M VM; Ning, Yu Y; Su, Fengyun F; Wang, Rui R; Stoffel, Elena M EM; Innis, Jeffrey W JW; Roberts, J Scott JS; Robertson, Patricia L PL; Yanik, Gregory G; Chamdin, Aghiad A; Connelly, James A JA; Choi, Sung S; Harris, Andrew C AC; Kitko, Carrie C; Rao, Rama Jasty RJ; Levine, John E JE; Castle, Valerie P VP; Hutchinson, Raymond J RJ; Talpaz, Moshe M; Robinson, Dan R DR; Chinnaiyan, Arul M AM
Publication Date: 2015-09-01

Variant appearance in text: NF1: E76Q
PubMed Link: 26325560
Variant Present in the following documents:
  • Main text
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