FAT1 c.266T>C ;(p.I89T)

Variant ID: 4-187630716-A-G

NM_005245.3(FAT1):c.266T>C;(p.I89T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.

Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31

Variant appearance in text: FAT1: I89T
PubMed Link: 33384420
Variant Present in the following documents:
  • Main text
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