TET2 c.1793del ;(p.N598Ifs*3)

Variant ID: 4-106156890-CA-C

NM_001127208.2(TET2):c.1793del;(p.N598Ifs*3)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study.

The Lancet. Haematology
,
Publication Date: 2022-11-24

Variant appearance in text: TET2: 1792del
PubMed Link: 36436542
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis.

Nature Genetics
Kar, Siddhartha P SP; Quiros, Pedro M PM; Gu, Muxin M; Jiang, Tao T; Mitchell, Jonathan J; Langdon, Ryan R; Iyer, Vivek V; Barcena, Clea C; Vijayabaskar, M S MS; Fabre, Margarete A MA; Carter, Paul P; Petrovski, Slavé S; Burgess, Stephen S; Vassiliou, George S GS
Publication Date: 2022-08

Variant appearance in text: TET2: N598Ifs*3
PubMed Link: 35835912
Variant Present in the following documents:
  • 41588_2022_1121_MOESM3_ESM.xlsx, sheet 4
View BVdb publication page



Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).

Clinical Lymphoma, Myeloma & Leukemia
DiNardo, Courtney D CD; Bannon, Sarah A SA; Routbort, Mark M; Franklin, Anna A; Mork, Maureen M; Armanios, Mary M; Mace, Emily M EM; Orange, Jordan S JS; Jeff-Eke, Meselle M; Churpek, Jane E JE; Takahashi, Koichi K; Jorgensen, Jeffrey L JL; Garcia-Manero, Guillermo G; Kornblau, Steve S; Bertuch, Alison A; Cheung, Hannah H; Bhalla, Kapil K; Futreal, Andrew A; Godley, Lucy A LA; Patel, Keyur P KP
Publication Date: 2016-07

Variant appearance in text: TET2: 1793del; N598fs
PubMed Link: 27210295
Variant Present in the following documents:
  • Main text
View BVdb publication page