ERBB2 c.2506C>T ;(p.L836=)

Variant ID: 17-37881314-C-T

NM_004448.2(ERBB2):c.2506C>T;(p.L836=)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.

International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017

Variant appearance in text: ERBB2: 2506C>T; Leu836Leu
PubMed Link: 31966388
Variant Present in the following documents:
  • Main text
View BVdb publication page



Amplicon sequencing of colorectal cancer: variant calling in frozen and formalin-fixed samples.

Plos One
Betge, Johannes J; Kerr, Grainne G; Miersch, Thilo T; Leible, Svenja S; Erdmann, Gerrit G; Galata, Christian L CL; Zhan, Tianzuo T; Gaiser, Timo T; Post, Stefan S; Ebert, Matthias P MP; Horisberger, Karoline K; Boutros, Michael M
Publication Date: 2015

Variant appearance in text: ERBB2: L836L
PubMed Link: 26010451
Variant Present in the following documents:
  • pone.0127146.s014.xlsx, sheet 3
View BVdb publication page



Detection of somatic mutations by high-resolution DNA melting (HRM) analysis in multiple cancers.

Plos One
Gonzalez-Bosquet, Jesus J; Calcei, Jacob J; Wei, Jun S JS; Garcia-Closas, Montserrat M; Sherman, Mark E ME; Hewitt, Stephen S; Vockley, Joseph J; Lissowska, Jolanta J; Yang, Hannah P HP; Khan, Javed J; Chanock, Stephen S
Publication Date: 2011-01-17

Variant appearance in text: rs104886008
PubMed Link: 21264207
Variant Present in the following documents:
View BVdb publication page