FAT1 c.9929G>A ;(p.G3310E)

Variant ID: 4-187531094-C-T

NM_005245.3(FAT1):c.9929G>A;(p.G3310E)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Recurrent somatic mutation of FAT1 in multiple human cancers leads to aberrant Wnt activation.

Nature Genetics
Morris, Luc G T LG; Kaufman, Andrew M AM; Gong, Yongxing Y; Ramaswami, Deepa D; Walsh, Logan A LA; Turcan, Şevin Ş; Eng, Stephanie S; Kannan, Kasthuri K; Zou, Yilong Y; Peng, Luke L; Banuchi, Victoria E VE; Paty, Phillip P; Zeng, Zhaoshi Z; Vakiani, Efsevia E; Solit, David D; Singh, Bhuvanesh B; Ganly, Ian I; Liau, Linda L; Cloughesy, Timothy C TC; Mischel, Paul S PS; Mellinghoff, Ingo K IK; Chan, Timothy A TA
Publication Date: 2013-03

Variant appearance in text: FAT1: Gly3310Glu
PubMed Link: 23354438
Variant Present in the following documents:
  • Main text
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