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TG c.2169dup ;(p.K724Qfs*12)
Variant ID: 8-133899783-G-GC
NM_003235.4(
TG
):c.2169dup;(p.K724Qfs*12)
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:
Gene-specific machine learning model to predict the pathogenicity of BRCA2 variants.
Frontiers In Genetics
Khandakji, Mohannad N MN; Mifsud, Borbala B
Publication Date: 2022
Variant appearance in text: TG: 2167dup
PubMed Link:
36246618
Variant Present in the following documents:
Table1.xlsx, sheet 3
View BVdb publication page
Haplotype-resolved de novo assembly of the Vero cell line genome.
Npj Vaccines
Sène, Marie-Angélique MA; Kiesslich, Sascha S; Djambazian, Haig H; Ragoussis, Jiannis J; Xia, Yu Y; Kamen, Amine A AA
Publication Date: 2021-08-20
Variant appearance in text: TG: 2168dupC
PubMed Link:
34417462
Variant Present in the following documents:
41541_2021_358_MOESM3_ESM.xlsx, sheet 1
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: 2167dup
PubMed Link:
32929070
Variant Present in the following documents:
41467_2020_18391_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page