FAT1 c.2656G>A ;(p.E886K)

Variant ID: 4-187628326-C-T

NM_005245.3(FAT1):c.2656G>A;(p.E886K)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Clinical genomic profiling of novel grey zone lymphoma paired lesions with sequential central nervous system involvement in two adolescent patients.

Haematologica
Benkli, Cagla Y CY; Marcogliese, Andrea N AN; Agrusa, Jennifer E JE; Adesina, Adekunle M AM; Weiner, Howard L HL; Fisher, Kevin E KE; Curry, Choladda V CV
Publication Date: 2021-09-01

Variant appearance in text: FAT1: 2656G>A; Glu886Lys
PubMed Link: 34162180
Variant Present in the following documents:
  • 1062533.pdf
View BVdb publication page