Bibliome.ai browser hg19
Search
About
Stats
FAQ
FAT1 c.3081G>T ;(p.E1027D)
Variant ID: 4-187627901-C-A
NM_005245.3(
FAT1
):c.3081G>T;(p.E1027D)
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:
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: E1027D
PubMed Link:
33384420
Variant Present in the following documents:
Main text
41598_2020_78370_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page