TET2 c.954del ;(p.K318Nfs*29)

Variant ID: 4-106156050-GA-G

NM_001127208.2(TET2):c.954del;(p.K318Nfs*29)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia.

Leukemia
Chase, Andrew A; Pellagatti, Andrea A; Singh, Shalini S; Score, Joannah J; Tapper, William J WJ; Lin, Feng F; Hoade, Yvette Y; Bryant, Catherine C; Trim, Nicola N; Yip, Bon Ham BH; Zoi, Katerina K; Rasi, Chiara C; Forsberg, Lars A LA; Dumanski, Jan P JP; Boultwood, Jacqueline J; Cross, Nicholas C P NCP
Publication Date: 2019-05

Variant appearance in text: TET2: K318Nfs*29
PubMed Link: 30573780
Variant Present in the following documents:
  • Main text
  • emss-79910.pdf
View BVdb publication page