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GC c.1131_1158del ;(p.D377Efs*7)
Variant ID: 4-72620701-CATTAAAACAGGTAGTTGAGTCTTCAACA-C
NM_000583.3(
GC
):c.1131_1158del;(p.D377Efs*7)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: 1131_1158del
PubMed Link:
33294491
Variant Present in the following documents:
mmc2.pdf
mmc1.pdf
View BVdb publication page