NF1 c.3301_3302del ;(p.Q1101Vfs*4)

Variant ID: 17-29559191-TCA-T

NM_001042492.2(NF1):c.3301_3302del;(p.Q1101Vfs*4)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical impact of a cancer genomic profiling test using an in-house comprehensive targeted sequencing system.

Cancer Science
Hayashi, Hideyuki H; Tanishima, Shigeki S; Fujii, Kyoko K; Mori, Ryo R; Okada, Chihiro C; Yanagita, Emmy E; Shibata, Yuka Y; Matsuoka, Ryosuke R; Amano, Toraji T; Yamada, Takahiro T; Yabe, Ichiro I; Kinoshita, Ichiro I; Komatsu, Yoshito Y; Dosaka-Akita, Hirotoshi H; Nishihara, Hiroshi H
Publication Date: 2020-10

Variant appearance in text: NF1: Q1101Vfs*4
PubMed Link: 32772458
Variant Present in the following documents:
  • CAS-111-3926-s001.xlsx, sheet 5
  • CAS-111-3926-s001.xlsx, sheet 4
View BVdb publication page