CELSR2 c.1331G>A ;(p.R444Q)

Variant ID: 1-109794032-G-A

NM_001408.2(CELSR2):c.1331G>A;(p.R444Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia.

Nature Communications
Ma, Xiaotu X; Edmonson, Michael M; Yergeau, Donald D; Muzny, Donna M DM; Hampton, Oliver A OA; Rusch, Michael M; Song, Guangchun G; Easton, John J; Harvey, Richard C RC; Wheeler, David A DA; Ma, Jing J; Doddapaneni, HarshaVardhan H; Vadodaria, Bhavin B; Wu, Gang G; Nagahawatte, Panduka P; Carroll, William L WL; Chen, I-Ming IM; Gastier-Foster, Julie M JM; Relling, Mary V MV; Smith, Malcolm A MA; Devidas, Meenakshi M; Guidry Auvil, Jaime M JM; Downing, James R JR; Loh, Mignon L ML; Willman, Cheryl L CL; Gerhard, Daniela S DS; Mullighan, Charles G CG; Hunger, Stephen P SP; Zhang, Jinghui J
Publication Date: 2015-03-19

Variant appearance in text: CELSR2: R444Q
PubMed Link: 25790293
Variant Present in the following documents:
  • ncomms7604-s3.xls, sheet 1
View BVdb publication page