NF1 c.1819_1821delinsTGT ;(p.R607C)

Variant ID: 17-29550559-AGG-TGT

NM_001042492.2(NF1):c.1819_1821delinsTGT;(p.R607C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Reliable Detection of Somatic Mutations in Fine Needle Aspirates of Pancreatic Cancer With Next-generation Sequencing: Implications for Surgical Management.

Annals Of Surgery
Valero, Vicente V; Saunders, Tyler J TJ; He, Jin J; Weiss, Matthew J MJ; Cameron, John L JL; Dholakia, Avani A; Wild, Aaron T AT; Shin, Eun Ji EJ; Khashab, Mouen A MA; O'Broin-Lennon, Anne Marie AM; Ali, Syed Z SZ; Laheru, Daniel D; Hruban, Ralph H RH; Iacobuzio-Donahue, Christine A CA; Herman, Joseph M JM; Wolfgang, Christopher L CL
Publication Date: 2016-01

Variant appearance in text: NF1: Arg607Cys
PubMed Link: 26020105
Variant Present in the following documents:
  • Main text
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