GC c.1165-35_1188del

Variant ID: 4-72620202-ATAGTTCCTTCTTTAGTAGAGGGCCCTGTAAGAAAACAATAATTGCATAACAAAATTATT-A

NM_000583.3(GC):c.1165-35_1188del

This variant was identified in 1 publication

View GRCh38 version.




Publications:


In Vitro and In Vivo Genetic Disease Modeling via NHEJ-Precise Deletions Using CRISPR-Cas9.

Molecular Therapy. Methods & Clinical Development
López-Manzaneda, Sergio S; Ojeda-Pérez, Isabel I; Zabaleta, Nerea N; García-Torralba, Aída A; Alberquilla, Omaira O; Torres, Raúl R; Sánchez-Domínguez, Rebeca R; Torella, Laura L; Olivier, Emmanuel E; Mountford, Joanne J; Ramírez, Juan C JC; Bueren, Juan A JA; González-Aseguinolaza, Gloria G; Segovia, Jose-Carlos JC
Publication Date: 2020-12-11

Variant appearance in text: GC: 1153_1189del
PubMed Link: 33294491
Variant Present in the following documents:
  • mmc1.pdf
  • mmc2.pdf
View BVdb publication page