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KMT2D c.16456G>A ;(p.V5486M)
Variant ID: 12-49415891-C-T
NM_003482.3(
KMT2D
):c.16456G>A;(p.V5486M)
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:
A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.
Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01
Variant appearance in text: KMT2D: V5486M
PubMed Link:
34963661
Variant Present in the following documents:
supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page
Histone modifier gene mutations in peripheral T-cell lymphoma not otherwise specified.
Haematologica
Ji, Meng-Meng MM; Huang, Yao-Hui YH; Huang, Jin-Yan JY; Wang, Zhao-Fu ZF; Fu, Di D; Liu, Han H; Liu, Feng F; Leboeuf, Christophe C; Wang, Li L; Ye, Jing J; Lu, Yi-Ming YM; Janin, Anne A; Cheng, Shu S; Zhao, Wei-Li WL
Publication Date: 2018-04
Variant appearance in text: KMT2D: V5486M
PubMed Link:
29305415
Variant Present in the following documents:
Main text
2017.182444.Ji_SUPPL.pdf
1030679.pdf
View BVdb publication page