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F8 c.493C>A ;(p.P165T)
Variant ID: X-154221319-G-T
NM_000132.3(
F8
):c.493C>A;(p.P165T)
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 prognostic risk model for glioma patients by systematic evaluation of genomic variations.
Iscience
Zhang, Baifeng B; Wan, Weiqing W; Li, Zibo Z; Gao, Zhixian Z; Ji, Nan N; Xie, Jian J; Wang, Junmei J; Wang, Bin B; Lai-Wan Kwong, Dora D; Guan, Xinyuan X; Gao, Shengjie S; Zhao, Yuanli Y; Lu, Youyong Y; Zhang, Liwei L; Rodland, Karin D KD; Tsang, Shirley X SX
Publication Date: 2022-12-22
Variant appearance in text: F8: P165T
PubMed Link:
36536675
Variant Present in the following documents:
mmc3.xls, sheet 1
View BVdb publication page
Prenatal Diagnosis of Glutaric Acidemia I Based on Amniotic Fluid Samples in 42 Families Using Genetic and Biochemical Approaches.
Frontiers In Genetics
Xiao, Bing B; Qiu, Wenjuan W; Ye, Jun J; Zhang, Huiwen H; Zhu, Hong H; Wang, Lei L; Liang, Lili L; Xu, Feng F; Chen, Ting T; Xu, Yan Y; Yu, Yongguo Y; Gu, Xuefan X; Han, Lianshu L
Publication Date: 2020
Variant appearance in text: F8: 493C>A
PubMed Link:
32508882
Variant Present in the following documents:
Main text
fgene-11-00496.pdf
View BVdb publication page