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RASIP1 c.823+1211G>C
Variant ID: 19-49241006-C-G
NM_017805.2(
RASIP1
):c.823+1211G>C
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:
Clinical and Genetic Risk Factors for Acute Incident Venous Thromboembolism in Ambulatory Patients With COVID-19.
Jama Internal Medicine
Xie, JunQing J; Prats-Uribe, Albert A; Feng, Qi Q; Wang, YunHe Y; Gill, Dipender D; Paredes, Roger R; Prieto-Alhambra, Dani D
Publication Date: 2022-10-01
Variant appearance in text: rs12981072
PubMed Link:
35980616
Variant Present in the following documents:
jamainternmed-e223858-s001.pdf
View BVdb publication page
Somatic Mutation Profiling of Papillary Thyroid Carcinomas by Whole-exome Sequencing and Its Relationship with Clinical Characteristics.
International Journal Of Medical Sciences
Qi, Tingyue T; Rong, Xin X; Feng, Qingling Q; Sun, Hongguang H; Cao, Haiyan H; Yang, Yan Y; Feng, Hao H; Zhu, Linhai L; Wang, Lei L; Du, Qiu Q
Publication Date: 2021
Variant appearance in text: rs12981072
PubMed Link:
34104084
Variant Present in the following documents:
ijmsv18p2532s2.xlsx, sheet 1
View BVdb publication page