TP53 c.1157A>T ;(p.K386M)

Variant ID: 17-7572952-T-A

NM_000546.5(TP53):c.1157A>T;(p.K386M)

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: TP53: 1157A>T; Lys386Met
PubMed Link: 29945233
Variant Present in the following documents:
  • bty518_supplementary_data_s2.xlsx, sheet 8
View BVdb publication page



iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers.

Scientific Reports
Wang, Meng M; Wei, Liping L
Publication Date: 2016-08-16

Variant appearance in text: TP53: K386M
PubMed Link: 27527004
Variant Present in the following documents:
  • srep31321-s5.xls, sheet 1
View BVdb publication page



Stat1 and SUMO modification.

Blood
Song, Li L; Bhattacharya, Samita S; Yunus, Ali A AA; Lima, Christopher D CD; Schindler, Christian C
Publication Date: 2006-11-15

Variant appearance in text: p53: K386M
PubMed Link: 16857984
Variant Present in the following documents:
  • Main text
View BVdb publication page