TET2 c.5300G>A ;(p.S1767N)

Variant ID: 4-106196967-G-A

NM_001127208.2(TET2):c.5300G>A;(p.S1767N)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis.

Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)
Martínez-Magaña, José J JJ; Genis-Mendoza, Alma D AD; González-Covarrubias, Vanessa V; Juárez-Rojop, Isela E IE; Tovilla-Zárate, Carlos A CA; Soberón, Xavier X; Lanzagorta, Nuria N; Nicolini, Humberto H
Publication Date: 2022

Variant appearance in text: TET2: Ser1767Asn
PubMed Link: 34037083
Variant Present in the following documents:
  • Main text
  • bjp-44-02-164.pdf
View BVdb publication page



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: 5300G>A; Ser1767Asn; rs185223849
PubMed Link: 31187595
Variant Present in the following documents:
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: 5300G>A; Ser1767Asn; rs185223849
PubMed Link: 29945233
Variant Present in the following documents:
  • bty518_supplementary_data_s6.xlsx, sheet 8
  • bty518_supplementary_data_s2.xlsx, sheet 8
View BVdb publication page