KCND2 c.1399G>T ;(p.V467F)

Variant ID: 7-120382588-G-T

NM_012281.2(KCND2):c.1399G>T;(p.V467F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The genomic and epigenomic evolutionary history of papillary renal cell carcinomas.

Nature Communications
Zhu, Bin B; Poeta, Maria Luana ML; Costantini, Manuela M; Zhang, Tongwu T; Shi, Jianxin J; Sentinelli, Steno S; Zhao, Wei W; Pompeo, Vincenzo V; Cardelli, Maurizio M; Alexandrov, Boian S BS; Otlu, Burcak B; Hua, Xing X; Jones, Kristine K; Brodie, Seth S; Dabrowska, Malgorzata Ewa ME; Toro, Jorge R JR; Yeager, Meredith M; Wang, Mingyi M; Hicks, Belynda B; Alexandrov, Ludmil B LB; Brown, Kevin M KM; Wedge, David C DC; Chanock, Stephen S; Fazio, Vito Michele VM; Gallucci, Michele M; Landi, Maria Teresa MT
Publication Date: 2020-06-18

Variant appearance in text: KCND2: V467F
PubMed Link: 32555180
Variant Present in the following documents:
  • 41467_2020_16546_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page