TET2 c.2079del ;(p.K693Nfs*7)

Variant ID: 4-106157173-GA-G

NM_001127208.2(TET2):c.2079del;(p.K693Nfs*7)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: 2079delA; Lys693fs
PubMed Link: 29945233
Variant Present in the following documents:
  • bty518_supplementary_data_s5.xlsx, sheet 8
  • bty518_supplementary_data_s10.xlsx, sheet 8
View BVdb publication page



Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy.

Biology Of Blood And Marrow Transplantation : Journal Of The American Society For Blood And Marrow Transplantation
Rojek, Katarzyna K; Nickels, Eric E; Neistadt, Barbara B; Marquez, Rafael R; Wickrema, Amittha A; Artz, Andrew A; van Besien, Koen K; Larson, Richard A RA; Lee, Ming K MK; Segal, Jeremy P JP; King, Mary-Claire MC; Walsh, Tom T; Shimamura, Akiko A; Keel, Sioban B SB; Churpek, Jane E JE; Godley, Lucy A LA
Publication Date: 2016-11

Variant appearance in text: TET2: 2079del; K693Nfs*7
PubMed Link: 27497531
Variant Present in the following documents:
  • Main text
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Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms.

Diagnostic Pathology
Au, Chun Hang CH; Wa, Anna A; Ho, Dona N DN; Chan, Tsun Leung TL; Ma, Edmond S K ES
Publication Date: 2016-01-22

Variant appearance in text: N/A
PubMed Link: 26796102
Variant Present in the following documents:
View BVdb publication page