TET2 c.4790del ;(p.F1597Sfs*13)

Variant ID: 4-106196455-CT-C

NM_001127208.2(TET2):c.4790del;(p.F1597Sfs*13)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The significance of genetic mutations and their prognostic impact on patients with incidental finding of isolated del(20q) in bone marrow without morphologic evidence of a myeloid neoplasm.

Blood Cancer Journal
Ravindran, Aishwarya A; He, Rong R; Ketterling, Rhett P RP; Jawad, Majd D MD; Chen, Dong D; Oliveira, Jennifer L JL; Nguyen, Phuong L PL; Viswanatha, David S DS; Reichard, Kaaren K KK; Hoyer, James D JD; Go, Ronald S RS; Shi, Min M
Publication Date: 2020-01-23

Variant appearance in text: TET2: 4790del; Phe1597Serfs*13
PubMed Link: 31974359
Variant Present in the following documents:
  • Main text
  • 41408_2020_Article_275.pdf
View BVdb publication page



appreci8: a pipeline for precise variant calling integrating 8 tools.

Bioinformatics (Oxford, England)
Sandmann, Sarah S; Karimi, Mohsen M; de Graaf, Aniek O AO; Rohde, Christian C; Göllner, Stefanie S; Varghese, Julian J; Ernsting, Jan J; Walldin, Gunilla G; van der Reijden, Bert A BA; Müller-Tidow, Carsten C; Malcovati, Luca L; Hellström-Lindberg, Eva E; Jansen, Joop H JH; Dugas, Martin M
Publication Date: 2018-12-15

Variant appearance in text: TET2: 4790delT; Phe1597fs
PubMed Link: 29945233
Variant Present in the following documents:
  • bty518_supplementary_data_s10.xlsx, sheet 8
View BVdb publication page