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SI c.1075_1077delinsTGA ;(p.R359*)
Variant ID: 3-164777759-GCG-TCA
NM_001041.3(
SI
):c.1075_1077delinsTGA;(p.R359*)
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:
Ilio-femoral venous thrombosis with hereditary antithrombin deficiency: a case report of rare thrombotic disease and successful treatment with catheter directed thrombolysis.
European Heart Journal. Case Reports
Miyashita, Hirokazu H; Tobita, Kazuki K; Morishita, Eriko E; Saito, Shigeru S
Publication Date: 2021-02
Variant appearance in text: SI: Arg359Ter
PubMed Link:
33738401
Variant Present in the following documents:
ytaa531.pdf
View BVdb publication page