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VWF c.5222T>C ;(p.I1741T)
Variant ID: 12-6125771-A-G
NM_000552.3(
VWF
):c.5222T>C;(p.I1741T)
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:
Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD.
Journal Of Thrombosis And Haemostasis : Jth
Flood, V H VH; Lederman, C A CA; Wren, J S JS; Christopherson, P A PA; Friedman, K D KD; Hoffmann, R G RG; Montgomery, R R RR
Publication Date: 2010-06
Variant appearance in text: VWF: I1741T
PubMed Link:
20345715
Variant Present in the following documents:
Main text
View BVdb publication page