NF1 c.1165C>T ;(p.H389Y)

Variant ID: 17-29528157-C-T

NM_001042492.2(NF1):c.1165C>T;(p.H389Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic and epigenetic characterization of posterior pituitary tumors.

Acta Neuropathologica
Schmid, Simone S; Solomon, David A DA; Perez, Eilis E; Thieme, Anne A; Kleinschmidt-DeMasters, Bette K BK; Giannini, Caterina C; Reinhardt, Annekathrin A; Asa, Sylvia L SL; Mete, Ozgur O; Stichel, Damian D; Siewert, Christin C; Dittmayer, Carsten C; Hasselblatt, Martin M; Paulus, Werner W; Nagel, Christoph C; Harter, Patrick N PN; Schittenhelm, Jens J; Honegger, Jürgen J; Rushing, Elisabeth E; Coras, Roland R; Pfister, Stefan M SM; Buslei, Rolf R; Koch, Arend A; Perry, Arie A; Jones, David T W DTW; von Deimling, Andreas A; Capper, David D; Lopes, M Beatriz MB
Publication Date: 2021-12

Variant appearance in text: NF1: 1165C>T; H389Y
PubMed Link: 34661724
Variant Present in the following documents:
  • Main text
  • 401_2021_2377_MOESM9_ESM.xlsx, sheet 1
  • 401_2021_Article_2377.pdf
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