NF1 c.331_332insTA ;(p.K111Ifs*55)

Variant ID: 17-29490245-C-CAT

NM_001042492.2(NF1):c.331_332insTA;(p.K111Ifs*55)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prevalence of disease-causing genes in Japanese patients with BRCA1/2-wildtype hereditary breast and ovarian cancer syndrome.

Npj Breast Cancer
Kaneyasu, Tomoko T; Mori, Seiichi S; Yamauchi, Hideko H; Ohsumi, Shozo S; Ohno, Shinji S; Aoki, Daisuke D; Baba, Shinichi S; Kawano, Junko J; Miki, Yoshio Y; Matsumoto, Naomichi N; Nagasaki, Masao M; Yoshida, Reiko R; Akashi-Tanaka, Sadako S; Iwase, Takuji T; Kitagawa, Dai D; Masuda, Kenta K; Hirasawa, Akira A; Arai, Masami M; Takei, Junko J; Ide, Yoshimi Y; Gotoh, Osamu O; Yaguchi, Noriko N; Nishi, Mitsuyo M; Kaneko, Keika K; Matsuyama, Yumi Y; Okawa, Megumi M; Suzuki, Misato M; Nezu, Aya A; Yokoyama, Shiro S; Amino, Sayuri S; Inuzuka, Mayuko M; Noda, Tetsuo T; Nakamura, Seigo S
Publication Date: 2020

Variant appearance in text: NF1: 331_332insTA; K111fs
PubMed Link: 32566746
Variant Present in the following documents:
  • Main text
  • 41523_2020_Article_163.pdf
  • 41523_2020_163_MOESM1_ESM.pdf
View BVdb publication page