TG c.2313dup ;(p.V772Sfs*8)

Variant ID: 8-133900363-C-CA

NM_003235.4(TG):c.2313dup;(p.V772Sfs*8)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Variation in targetable genomic alterations in non-small cell lung cancer by genetic ancestry, sex, smoking history, and histology.

Genome Medicine
Adib, Elio E; Nassar, Amin H AH; Abou Alaiwi, Sarah S; Groha, Stefan S; Akl, Elie W EW; Sholl, Lynette M LM; Michael, Kesi S KS; Awad, Mark M MM; Jӓnne, Pasi A PA; Gusev, Alexander A; Kwiatkowski, David J DJ
Publication Date: 2022-04-15

Variant appearance in text: TG: 2312dup
PubMed Link: 35428358
Variant Present in the following documents:
  • 13073_2022_1041_MOESM2_ESM.xlsx, sheet 2
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: 2313dup
PubMed Link: 34417462
Variant Present in the following documents:
  • 41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page