ERBB2 c.2279C>T ;(p.S760F)

Variant ID: 17-37880235-C-T

NM_004448.2(ERBB2):c.2279C>T;(p.S760F)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


ERBB2 mutation is associated with sustained tumor cell proliferation after short-term preoperative endocrine therapy in early lobular breast cancer.

Modern Pathology : An Official Journal Of The United States And Canadian Academy Of Pathology, Inc
Grote, Isabel I; Bartels, Stephan S; Christgen, Henriette H; Radner, Martin M; Gronewold, Malte M; Kandt, Leonie L; Raap, Mieke M; Lehmann, Ulrich U; Gluz, Oleg O; Graeser, Monika M; Kuemmel, Sherko S; Nitz, Ulrike U; Harbeck, Nadia N; Kreipe, Hans H; Christgen, Matthias M
Publication Date: 2022-12

Variant appearance in text: ERBB2: S760F
PubMed Link: 35842479
Variant Present in the following documents:
  • 41379_2022_1130_MOESM1_ESM.pdf
View BVdb publication page



TP53 mutations are associated with primary endocrine resistance in luminal early breast cancer.

Cancer Medicine
Grote, Isabel I; Bartels, Stephan S; Kandt, Leonie L; Bollmann, Laura L; Christgen, Henriette H; Gronewold, Malte M; Raap, Mieke M; Lehmann, Ulrich U; Gluz, Oleg O; Nitz, Ulrike U; Kuemmel, Sherko S; Zu Eulenburg, Christine C; Braun, Michael M; Aktas, Bahriye B; Grischke, Eva-Maria EM; Schumacher, Claudia C; Luedtke-Heckenkamp, Kerstin K; Kates, Ronald R; Wuerstlein, Rachel R; Graeser, Monika M; Harbeck, Nadia N; Christgen, Matthias M; Kreipe, Hans H
Publication Date: 2021-12

Variant appearance in text: ERBB2: 2279C>T; S760F
PubMed Link: 34779146
Variant Present in the following documents:
  • CAM4-10-8581-s002.xlsx, sheet 1
View BVdb publication page



TP53 mutations are associated with primary endocrine resistance in luminal early breast cancer.

Cancer Medicine
Grote, Isabel I; Bartels, Stephan S; Kandt, Leonie L; Bollmann, Laura L; Christgen, Henriette H; Gronewold, Malte M; Raap, Mieke M; Lehmann, Ulrich U; Gluz, Oleg O; Nitz, Ulrike U; Kuemmel, Sherko S; Zu Eulenburg, Christine C; Braun, Michael M; Aktas, Bahriye B; Grischke, Eva-Maria EM; Schumacher, Claudia C; Luedtke-Heckenkamp, Kerstin K; Kates, Ronald R; Wuerstlein, Rachel R; Graeser, Monika M; Harbeck, Nadia N; Christgen, Matthias M; Kreipe, Hans H
Publication Date: 2021-12

Variant appearance in text: ERBB2: 2279C>T; S760F
PubMed Link: 34779146
Variant Present in the following documents:
  • CAM4-10-8581-s002.xlsx, sheet 1
View BVdb publication page



Application of a multi-gene next-generation sequencing panel to a non-invasive oesophageal cell-sampling device to diagnose dysplastic Barrett's oesophagus.

The Journal Of Pathology. Clinical Research
Katz-Summercorn, Annalise A; Anand, Shubha S; Ingledew, Sophie S; Huang, Yuanxue Y; Roberts, Thomas T; Galeano-Dalmau, Nuria N; O'Donovan, Maria M; Liu, Hongxiang H; Fitzgerald, Rebecca C RC
Publication Date: 2017-10

Variant appearance in text: ERBB2: 2279C>T
PubMed Link: 29085666
Variant Present in the following documents:
  • CJP2-3-258-s004.xlsx, sheet 1
View BVdb publication page