Bibliome.ai browser hg19
Search
About
Stats
FAQ
TG c.3367G>T ;(p.G1123C)
Variant ID: 8-133912518-G-T
NM_003235.4(
TG
):c.3367G>T;(p.G1123C)
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:
Type 1 Diabetes and Autoimmune Thyroid Disease-The Genetic Link.
Frontiers In Endocrinology
Frommer, Lara L; Kahaly, George J GJ
Publication Date: 2021
Variant appearance in text: TG: G1123C
PubMed Link:
33776915
Variant Present in the following documents:
Main text
fendo-12-618213.pdf
View BVdb publication page
Precise allele-specific genome editing by spatiotemporal control of CRISPR-Cas9 via pronuclear transplantation.
Nature Communications
Li, Yanhe Y; Weng, Yuteng Y; Bai, Dandan D; Jia, Yanping Y; Liu, Yingdong Y; Zhang, Yalin Y; Kou, Xiaochen X; Zhao, Yanhong Y; Ruan, Jingling J; Chen, Jiayu J; Yin, Jiqing J; Wang, Hong H; Teng, Xiaoming X; Wang, Zuolin Z; Liu, Wenqiang W; Gao, Shaorong S
Publication Date: 2020-09-14
Variant appearance in text: TG: 3367G>T
PubMed Link:
32929070
Variant Present in the following documents:
41467_2020_18391_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page