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SREBF2 c.2738+465C>G
Variant ID: 22-42295250-C-G
NM_004599.3(
SREBF2
):c.2738+465C>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
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: rs713881
PubMed Link:
34104084
Variant Present in the following documents:
ijmsv18p2532s2.xlsx, sheet 1
View BVdb publication page
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: rs713881
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page
Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22.
Human Genomics
González-Neira, Anna A; Calafell, Francesc F; Navarro, Arcadi A; Lao, Oscar O; Cann, Howard H; Comas, David D; Bertranpetit, Jaume J
Publication Date: 2004-11
Variant appearance in text: rs713881
PubMed Link:
15606995
Variant Present in the following documents:
Main text
1479-7364-1-6-399.pdf
View BVdb publication page