PALB2 c.1368G>C ;(p.E456D)

Variant ID: 16-23646499-C-G

NM_024675.3(PALB2):c.1368G>C;(p.E456D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


BRCA2, EGFR, and NTRK mutations in mismatch repair-deficient colorectal cancers with MSH2 or MLH1 mutations.

Oncotarget
Deihimi, Safoora S; Lev, Avital A; Slifker, Michael M; Shagisultanova, Elena E; Xu, Qifang Q; Jung, Kyungsuk K; Vijayvergia, Namrata N; Ross, Eric A EA; Xiu, Joanne J; Swensen, Jeffrey J; Gatalica, Zoran Z; Andrake, Mark M; Dunbrack, Roland L RL; El-Deiry, Wafik S WS
Publication Date: 2017-06-20

Variant appearance in text: N/A
PubMed Link: 28591715
Variant Present in the following documents:
View BVdb publication page