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FAT1 c.289_291delinsTGT ;(p.R97C)
Variant ID: 4-187630691-TCT-ACA
NM_005245.3(
FAT1
):c.289_291delinsTGT;(p.R97C)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Construction and validation of an immunoediting-based optimized neoantigen load (ioTNL) model to predict the response and prognosis of immune checkpoint therapy in various cancers.
Aging
Su, Xiaofan X; Jin, Haoxuan H; Wang, Jiaqian J; Lu, Huiping H; Gu, Tiantian T; Gao, Zhibo Z; Li, Manxiang M
Publication Date: 2022-05-25
Variant appearance in text: FAT1: R97C
PubMed Link:
35613927
Variant Present in the following documents:
aging-14-204101-s004.xlsx, sheet 1
View BVdb publication page
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: R97C
PubMed Link:
33384420
Variant Present in the following documents:
Main text
View BVdb publication page