Bibliome.ai browser hg19
Search
About
Stats
FAQ
DDX10 c.1427T>C ;(p.V476A)
Variant ID: 11-108590540-T-C
NM_004398.2(
DDX10
):c.1427T>C;(p.V476A)
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:
Systematic assessment and optimizing algorithm of tumor mutational burden calculation and their implications in clinical decision-making.
Frontiers In Oncology
Sun, Daqiang D; Xu, Meilin M; Pan, Chaohu C; Tang, Hongzhen H; Wang, Peng P; Wu, Dongfang D; Luo, Haitao H
Publication Date: 2022
Variant appearance in text: DDX10: 1427T>C
PubMed Link:
36425562
Variant Present in the following documents:
Table_3.xlsx, sheet 1
Table_5.xlsx, sheet 1
Table_4.xlsx, sheet 1
View BVdb publication page
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: DDX10: 1427T>C; V476A
PubMed Link:
35613927
Variant Present in the following documents:
aging-14-204101-s004.xlsx, sheet 1
View BVdb publication page