ERBB2 c.50C>T ;(p.P17L)

Variant ID: 17-37856541-C-T

NM_004448.2(ERBB2):c.50C>T;(p.P17L)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.

Nature Communications
Havugimana, Pierre C PC; Goel, Raghuveera Kumar RK; Phanse, Sadhna S; Youssef, Ahmed A; Padhorny, Dzmitry D; Kotelnikov, Sergei S; Kozakov, Dima D; Emili, Andrew A
Publication Date: 2022-07-13

Variant appearance in text: ERBB2: 50C>T
PubMed Link: 35831314
Variant Present in the following documents:
  • 41467_2022_31809_MOESM8_ESM.xlsx, sheet 3
View BVdb publication page



Impact of genetic polymorphisms on adenoma recurrence and toxicity in a COX2 inhibitor (celecoxib) trial: results from a pilot study.

Pharmacogenetics And Genomics
Kraus, Sarah S; Hummler, Simone S; Toriola, Adetunji T AT; Poole, Elizabeth M EM; Scherer, Dominique D; Kotzmann, Jana J; Makar, Karen W KW; Kazanov, Dina D; Galazan, Lior L; Naumov, Inna I; Coghill, Anna E AE; Duggan, David D; Gigic, Biljana B; Arber, Nadir N; Ulrich, Cornelia M CM
Publication Date: 2013-08

Variant appearance in text: HER2: P17L
PubMed Link: 23778325
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacogenetics and stroke.

Stroke
Meschia, James F JF
Publication Date: 2009-11

Variant appearance in text: HER2: Pro17Leu
PubMed Link: 19762696
Variant Present in the following documents:
  • Main text
View BVdb publication page