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KMT2C c.5694T>C ;(p.Y1898=)
Variant ID: 7-151879251-A-G
NM_170606.2(
KMT2C
):c.5694T>C;(p.Y1898=)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Predictive mutation signature of immunotherapy benefits in NSCLC based on machine learning algorithms.
Frontiers In Immunology
Liu, Zhichao Z; Lin, Guo G; Yan, Zeping Z; Li, Linduo L; Wu, Xingchen X; Shi, Jingrong J; He, Jianxing J; Zhao, Lei L; Liang, Hengrui H; Wang, Wei W
Publication Date: 2022
Variant appearance in text: MLL3: 5694T>C; Y1898Y
PubMed Link:
36238300
Variant Present in the following documents:
Table_1.xlsx, sheet 4
View BVdb publication page
EPHA5 mutation was associated with adverse outcome of atezolizumab treatment in late-stage non-small cell lung cancers.
Bmc Pulmonary Medicine
Li, Zhenxiang Z; Zhou, Qing Q; Wang, Qi Q; Wang, Haiyong H; Yue, Weiming W
Publication Date: 2022-09-19
Variant appearance in text: MLL3: 5694T>C; Y1898Y
PubMed Link:
36123678
Variant Present in the following documents:
12890_2022_2161_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
Utility of exome sequencing in routine care for metastatic colorectal cancer.
Molecular And Clinical Oncology
D'Agay, Melchior De Giraud MG; Galland, Loïck L; Tharin, Zoe Z; Truntzer, Caroline C; Ghiringhelli, Francois F
Publication Date: 2021-11
Variant appearance in text: KMT2C: 5694T>C; Tyr1898=
PubMed Link:
34631054
Variant Present in the following documents:
Supplementary_Data.pdf
View BVdb publication page