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GOT2 c.296T>C ;(p.I99T)
Variant ID: 16-58756133-A-G
NM_002080.2(
GOT2
):c.296T>C;(p.I99T)
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:
Mutational Profile and Potential Molecular Therapeutic Targets of Pheochromocytoma.
Frontiers In Endocrinology
Ma, Xiaosen X; Ling, Chao C; Zhao, Meng M; Wang, Fen F; Cui, Yunying Y; Wen, Jin J; Ji, Zhigang Z; Zhang, Caili C; Chen, Shi S; Tong, Anli A; Li, Yuxiu Y
Publication Date: 2022
Variant appearance in text: GOT2: I99T; rs982114598
PubMed Link:
35966080
Variant Present in the following documents:
Table_1.xlsx, sheet 5
View BVdb publication page