VCAN c.3025C>T ;(p.Q1009*)

Variant ID: 5-82817150-C-T

NM_004385.4(VCAN):c.3025C>T;(p.Q1009*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted sequencing using a 47 gene multiple myeloma mutation panel (M(3) P) in -17p high risk disease.

British Journal Of Haematology
Kortüm, Klaus M KM; Langer, Christian C; Monge, Jorge J; Bruins, Laura L; Egan, Jan B JB; Zhu, Yuan X YX; Shi, Chang Xin CX; Jedlowski, Patrick P; Schmidt, Jessica J; Ojha, Juhi J; Bullinger, Lars L; Liebisch, Peter P; Kull, Miriam M; Champion, Mia D MD; Van Wier, Scott S; Ahmann, Gregory G; Rasche, Leo L; Knop, Stefan S; Fonseca, Rafael R; Einsele, Hermann H; Stewart, A Keith AK; Braggio, Esteban E
Publication Date: 2015-02

Variant appearance in text: VCAN: Gln1009*
PubMed Link: 25302557
Variant Present in the following documents:
  • Main text
View BVdb publication page