NF1 c.6862_6866del ;(p.Q2288Sfs*17)

Variant ID: 17-29665760-CAGTCA-C

NM_001042492.2(NF1):c.6862_6866del;(p.Q2288Sfs*17)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Analytical Validation of the Next-Generation Sequencing Assay for a Nationwide Signal-Finding Clinical Trial: Molecular Analysis for Therapy Choice Clinical Trial.

The Journal Of Molecular Diagnostics : Jmd
Lih, Chih-Jian CJ; Harrington, Robin D RD; Sims, David J DJ; Harper, Kneshay N KN; Bouk, Courtney H CH; Datta, Vivekananda V; Yau, Jonathan J; Singh, Rajesh R RR; Routbort, Mark J MJ; Luthra, Rajyalakshmi R; Patel, Keyur P KP; Mantha, Geeta S GS; Krishnamurthy, Savitri S; Ronski, Karyn K; Walther, Zenta Z; Finberg, Karin E KE; Canosa, Sandra S; Robinson, Hayley H; Raymond, Amelia A; Le, Long P LP; McShane, Lisa M LM; Polley, Eric C EC; Conley, Barbara A BA; Doroshow, James H JH; Iafrate, A John AJ; Sklar, Jeffrey L JL; Hamilton, Stanley R SR; Williams, P Mickey PM
Publication Date: 2017-03

Variant appearance in text: NF1: 6859_6863delAGTCA
PubMed Link: 28188106
Variant Present in the following documents:
  • Main text
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