NF1 c.4172C>A ;(p.S1391*)

Variant ID: 17-29580017-C-A

NM_001042492.2(NF1):c.4172C>A;(p.S1391*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinically Integrated Sequencing Alters Therapy in Children and Young Adults With High-Risk Glial Brain Tumors.

Jco Precision Oncology
Koschmann, Carl C; Wu, Yi-Mi YM; Kumar-Sinha, Chandan C; Lonigro, Robert R; Vats, Pankaj P; Kasaian, Katayoon K; Cieslik, Marcin M; Cao, Xuhong X; Anderson, Bailey B; Frank, Kevin K; Zhao, Lili L; Prensner, John R JR; Zureick, Andrew H AH; Everett, Jessica J; Mullan, Brendan B; Marini, Bernard B; Camelo-Piragua, Sandra S; Venneti, Sriram S; McKeever, Paul P; McFadden, Kathryn K; Lieberman, Andrew P AP; Leonard, Marcia M; Maher, Cormac O CO; Garton, Hugh H; Muraszko, Karin K; Robertson, Patricia P; Robinson, Dan D; Chinnaiyan, Arul M AM; Mody, Rajen R
Publication Date: 2018

Variant appearance in text: NF1: S1391*
PubMed Link: 32832832
Variant Present in the following documents:
  • Main text
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