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PC c.349_352del ;(p.G117Tfs*87)
Variant ID: 11-66638920-TAGCC-T
NM_001040716.1(
PC
):c.349_352del;(p.G117Tfs*87)
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:
Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.
Plos One
Tang, Liang L; Guo, Tao T; Yang, Rui R; Mei, Heng H; Wang, Huafang H; Lu, Xuan X; Yu, Jianming J; Wang, Qingyun Q; Hu, Yu Y
Publication Date: 2012
Variant appearance in text: PC: 349_352del
PubMed Link:
22545135
Variant Present in the following documents:
Main text
pone.0035773.pdf
View BVdb publication page