ERBB2 c.1926_1946+15del

Variant ID: 17-37876067-GCCCCGCCGAGCAGAGAGCCAGGTTGGCCTGGACCCC-G

NM_004448.2(ERBB2):c.1926_1946+15del

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical significance of ERBB2 exon 16 skipping: analysis of a real-world retrospective observational cohort study.

Esmo Open
Shi, Lei L; Xu, Caihua C; Ma, Yutong Y; Ou, Qiuxiang Q; Wu, Xue X; Lu, Songhua S; Shao, Yang Y; Guo, Renhua R; Kong, Jinliang J
Publication Date: 2020-11

Variant appearance in text: ERBB2: 1926_1946+15del
PubMed Link: 33214226
Variant Present in the following documents:
  • esmoopen-2020-000985supp001.pdf
View BVdb publication page