BRAF c.1507G>C ;(p.G503R)

Variant ID: 7-140477801-C-G

NM_004333.4(BRAF):c.1507G>C;(p.G503R)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Molecular signaling in multiple myeloma: association of RAS/RAF mutations and MEK/ERK pathway activation.

Oncogenesis
Xu, J J; Pfarr, N N; Endris, V V; Mai, E K EK; Md Hanafiah, N H NH; Lehners, N N; Penzel, R R; Weichert, W W; Ho, A D AD; Schirmacher, P P; Goldschmidt, H H; Andrulis, M M; Raab, M S MS
Publication Date: 2017-05-15

Variant appearance in text: BRAF: G503R
PubMed Link: 28504689
Variant Present in the following documents:
  • oncsis201736x2.pdf
View BVdb publication page



Targeted sequencing of refractory myeloma reveals a high incidence of mutations in CRBN and Ras pathway genes.

Blood
Kortüm, K Martin KM; Mai, Elias K EK; Hanafiah, Nur H NH; Shi, Chang-Xi CX; Zhu, Yuan-Xiao YX; Bruins, Laura L; Barrio, Santiago S; Jedlowski, Patrick P; Merz, Maximilian M; Xu, Jing J; Stewart, Robert A RA; Andrulis, Mindaugas M; Jauch, Anna A; Hillengass, Jens J; Goldschmidt, Hartmut H; Bergsagel, P Leif PL; Braggio, Esteban E; Stewart, A Keith AK; Raab, Marc S MS
Publication Date: 2016-09-01

Variant appearance in text: BRAF: Gly503Arg
PubMed Link: 27458004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes.

British Journal Of Cancer
Kratz, C P CP; Franke, L L; Peters, H H; Kohlschmidt, N N; Kazmierczak, B B; Finckh, U U; Bier, A A; Eichhorn, B B; Blank, C C; Kraus, C C; Kohlhase, J J; Pauli, S S; Wildhardt, G G; Kutsche, K K; Auber, B B; Christmann, A A; Bachmann, N N; Mitter, D D; Cremer, F W FW; Mayer, K K; Daumer-Haas, C C; Nevinny-Stickel-Hinzpeter, C C; Oeffner, F F; Schlüter, G G; Gencik, M M; Überlacker, B B; Lissewski, C C; Schanze, I I; Greene, M H MH; Spix, C C; Zenker, M M
Publication Date: 2015-04-14

Variant appearance in text: BRAF: G503R
PubMed Link: 25742478
Variant Present in the following documents:
  • bjc201575a.pdf
View BVdb publication page



Twin infant with lymphatic dysplasia diagnosed with Noonan syndrome by molecular genetic testing.

Fetal And Pediatric Pathology
Mathur, Deepan D; Somashekar, Santhosh S; Navarrete, Cristina C; Rodriguez, Maria M MM
Publication Date: 2014-08

Variant appearance in text: BRAF: 1507G>C; G503R
PubMed Link: 24754368
Variant Present in the following documents:
  • PDP-33-253.pdf
View BVdb publication page



Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome.

Oncology Reports
Timeus, Fabio F; Crescenzio, Nicoletta N; Baldassarre, Giuseppina G; Doria, Alessandra A; Vallero, Stefano S; Foglia, Luiselda L; Pagliano, Sara S; Rossi, Cesare C; Silengo, Margherita Cirillo MC; Ramenghi, Ugo U; Fagioli, Franca F; Cordero di Montezemolo, Luca L; Ferrero, Giovanni Battista GB
Publication Date: 2013-08

Variant appearance in text: BRAF: Gly503Arg
PubMed Link: 23756559
Variant Present in the following documents:
  • or-30-02-0553.pdf
View BVdb publication page