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TF c.112T>C ;(p.C38R)
Variant ID: 3-133467324-T-C
NM_001063.3(
TF
):c.112T>C;(p.C38R)
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:
Why factor XI deficiency is a clinical concern.
Expert Review Of Hematology
Wheeler, Allison P AP; Gailani, David D
Publication Date: 2016-07
Variant appearance in text: TF: Cys38Arg
PubMed Link:
27216469
Variant Present in the following documents:
Main text
View BVdb publication page
Advances in dynamic modeling of colorectal cancer signaling-network regions, a path toward targeted therapies.
Oncotarget
Tortolina, Lorenzo L; Duffy, David J DJ; Maffei, Massimo M; Castagnino, Nicoletta N; Carmody, Aimée M AM; Kolch, Walter W; Kholodenko, Boris N BN; De Ambrosi, Cristina C; Barla, Annalisa A; Biganzoli, Elia M EM; Nencioni, Alessio A; Patrone, Franco F; Ballestrero, Alberto A; Zoppoli, Gabriele G; Verri, Alessandro A; Parodi, Silvio S
Publication Date: 2015-03-10
Variant appearance in text: TF: c38r
PubMed Link:
25671297
Variant Present in the following documents:
oncotarget-06-5041-s001.pdf
View BVdb publication page