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TG c.2148_2149del ;(p.R717Kfs*18)
Variant ID: 8-133899763-ACT-A
NM_003235.4(
TG
):c.2148_2149del;(p.R717Kfs*18)
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:
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: 2147_2148del
PubMed Link:
32929070
Variant Present in the following documents:
41467_2020_18391_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
Gene panel screening for insight towards breast cancer susceptibility in different ethnicities.
Plos One
Bishop, Madison R MR; Omeler-Fenaud, Sophonie M SM; Huskey, Anna L W ALW; Merner, Nancy D ND
Publication Date: 2020
Variant appearance in text: TG: 2148_2149del
PubMed Link:
32866190
Variant Present in the following documents:
Main text
pone.0238295.pdf
View BVdb publication page