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VWF c.4192G>A ;(p.V1398I)
Variant ID: 12-6128392-C-T
NM_000552.3(
VWF
):c.4192G>A;(p.V1398I)
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:
Multiscale heterogeneity in gastric adenocarcinoma evolution is an obstacle to precision medicine.
Genome Medicine
Röcken, Christoph C; Amallraja, Anu A; Halske, Christine C; Opasic, Luka L; Traulsen, Arne A; Behrens, Hans-Michael HM; Krüger, Sandra S; Liu, Anne A; Haag, Jochen J; Egberts, Jan-Hendrik JH; Rosenstiel, Philip P; Meißner, Tobias T
Publication Date: 2021-11-08
Variant appearance in text: VWF: V1398I
PubMed Link:
34749812
Variant Present in the following documents:
13073_2021_975_MOESM2_ESM.xlsx, sheet 6
13073_2021_975_MOESM2_ESM.xlsx, sheet 12
View BVdb publication page
Structural basis of regulation of von Willebrand factor binding to glycoprotein Ib.
The Journal Of Biological Chemistry
Blenner, Mark A MA; Dong, Xianchi X; Springer, Timothy A TA
Publication Date: 2014-02-28
Variant appearance in text: VWF: V1398I
PubMed Link:
24391089
Variant Present in the following documents:
Main text
View BVdb publication page