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VWF c.7332G>A ;(p.W2444*)
Variant ID: 12-6085382-C-T
NM_000552.3(
VWF
):c.7332G>A;(p.W2444*)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
[Mutation analysis of VWF gene in two patients with von Willebrand disease by target sequence capture and high-throughput sequencing technology].
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi
Feng, Y Y; Mei, S Y SY; Liu, N N; Guo, R X RX
Publication Date: 2018-03-14
Variant appearance in text: VWF: 7332G>A; W2444X
PubMed Link:
29562472
Variant Present in the following documents:
Main text
cjh-39-03-242.pdf
View BVdb publication page