DNAH11 c.1987C>G ;(p.P663A)

Variant ID: 7-21628839-C-G

NM_001277115.1(DNAH11):c.1987C>G;(p.P663A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of recurrent FHL2-GLI2 oncogenic fusion in sclerosing stromal tumors of the ovary.

Nature Communications
Kim, Sarah H SH; Da Cruz Paula, Arnaud A; Basili, Thais T; Dopeso, Higinio H; Bi, Rui R; Pareja, Fresia F; da Silva, Edaise M EM; Gularte-Mérida, Rodrigo R; Sun, Zhen Z; Fujisawa, Sho S; Smith, Caitlin G CG; Ferrando, Lorenzo L; Martins Sebastião, Ana Paula AP; Bykov, Yonina Y; Li, Anqi A; Silveira, Catarina C; Ashley, Charles W CW; Stylianou, Anthe A; Selenica, Pier P; Samore, Wesley R WR; Jungbluth, Achim A AA; Zamarin, Dmitriy D; Abu-Rustum, Nadeem R NR; Helin, Kristian K; Soslow, Robert A RA; Reis-Filho, Jorge S JS; Oliva, Esther E; Weigelt, Britta B
Publication Date: 2020-01-02

Variant appearance in text: DNAH11: P663A
PubMed Link: 31896750
Variant Present in the following documents:
  • 41467_2019_13806_MOESM1_ESM.pdf
View BVdb publication page