TET2 c.3991A>C ;(p.T1331P)

Variant ID: 4-106182952-A-C

NM_001127208.2(TET2):c.3991A>C;(p.T1331P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


TET2 missense variants in human neoplasia. A proposal of structural and functional classification.

Molecular Genetics & Genomic Medicine
Bussaglia, Elena E; Antón, Rosa R; Nomdedéu, Josep F JF; Fuentes-Prior, Pablo P
Publication Date: 2019-07

Variant appearance in text: TET2: 3991A>C; Thr1331Pro
PubMed Link: 31187595
Variant Present in the following documents:
View BVdb publication page



Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesis.

Nature Genetics
Busque, Lambert L; Patel, Jay P JP; Figueroa, Maria E ME; Vasanthakumar, Aparna A; Provost, Sylvie S; Hamilou, Zineb Z; Mollica, Luigina L; Li, Juan J; Viale, Agnes A; Heguy, Adriana A; Hassimi, Maryam M; Socci, Nicholas N; Bhatt, Parva K PK; Gonen, Mithat M; Mason, Christopher E CE; Melnick, Ari A; Godley, Lucy A LA; Brennan, Cameron W CW; Abdel-Wahab, Omar O; Levine, Ross L RL
Publication Date: 2012-11

Variant appearance in text: TET2: 3991A>C; Thr1331Pro
PubMed Link: 23001125
Variant Present in the following documents:
  • Main text
  • NIHMS403965-supplement-1.pdf
  • nihms403965.pdf
View BVdb publication page