HR c.715_717delinsTGG ;(p.R239W)

Variant ID: 8-21985238-TCT-CCA

NM_005144.4(HR):c.715_717delinsTGG;(p.R239W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis.

Blood
Jerez, Andres A; Sugimoto, Yuka Y; Makishima, Hideki H; Verma, Amit A; Jankowska, Anna M AM; Przychodzen, Bartlomiej B; Visconte, Valeria V; Tiu, Ramon V RV; O'Keefe, Christine L CL; Mohamedali, Azim M AM; Kulasekararaj, Austin G AG; Pellagatti, Andrea A; McGraw, Kathy K; Muramatsu, Hideki H; Moliterno, Alison R AR; Sekeres, Mikkael A MA; McDevitt, Michael A MA; Kojima, Seiji S; List, Alan A; Boultwood, Jacqueline J; Mufti, Ghulam J GJ; Maciejewski, Jaroslaw P JP
Publication Date: 2012-06-21

Variant appearance in text: HR: R239W
PubMed Link: 22553315
Variant Present in the following documents:
  • Main text
View BVdb publication page