BRCA2 c.2367_2368insT ;(p.E790*)

Variant ID: 13-32910859-A-AT

NM_000059.3(BRCA2):c.2367_2368insT;(p.E790*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Simultaneous detection of genetic and copy number alterations in BRCA1/2 genes.

Oncotarget
Hirotsu, Yosuke Y; Ooka, Yoshihiko Y; Sakamoto, Ikuko I; Nakagomi, Hiroshi H; Omata, Masao M
Publication Date: 2017-12-29

Variant appearance in text: N/A
PubMed Link: 29383094
Variant Present in the following documents:
View BVdb publication page