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MED23 c.4078G>A ;(p.V1360M)
Variant ID: 6-131908848-C-T
NM_004830.3(
MED23
):c.4078G>A;(p.V1360M)
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:
Identification of biomarkers complementary to homologous recombination deficiency for improving the clinical outcome of ovarian serous cystadenocarcinoma.
Clinical And Translational Medicine
Shi, Zhiwen Z; Zhao, Qingguo Q; Lv, Bin B; Qu, Xinyu X; Han, Xiao X; Wang, Hongyan H; Qiu, Junjun J; Hua, Keqin K
Publication Date: 2021-05
Variant appearance in text: MED23: 4078G>A; V1360M
PubMed Link:
34047476
Variant Present in the following documents:
CTM2-11-e399-s003.xls, sheet 1
View BVdb publication page
Integrated multi-omics analysis of genomics, epigenomics, and transcriptomics in ovarian carcinoma.
Aging
Zheng, Mingjun M; Hu, Yuexin Y; Gou, Rui R; Wang, Jing J; Nie, Xin X; Li, Xiao X; Liu, Qing Q; Liu, Juanjuan J; Lin, Bei B
Publication Date: 2019-06-29
Variant appearance in text: MED23: 4078G>A
PubMed Link:
31257224
Variant Present in the following documents:
aging-11-102047-s002.xlsx, sheet 11
View BVdb publication page