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PC c.2563_2564delinsGC ;(p.K855A)
Variant ID: 11-66617845-TT-GC
NM_001040716.1(
PC
):c.2563_2564delinsGC;(p.K855A)
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:
Enhanced specificity mutations perturb allosteric signaling in CRISPR-Cas9.
Elife
Nierzwicki, Lukasz L; East, Kyle W KW; Morzan, Uriel N UN; Arantes, Pablo R PR; Batista, Victor S VS; Lisi, George P GP; Palermo, Giulia G
Publication Date: 2021-12-15
Variant appearance in text: PC: K855A
PubMed Link:
34908530
Variant Present in the following documents:
elife-73601.pdf
View BVdb publication page
Enhanced specificity mutations perturb allosteric signaling in CRISPR-Cas9.
Elife
Nierzwicki, Lukasz L; East, Kyle W KW; Morzan, Uriel N UN; Arantes, Pablo R PR; Batista, Victor S VS; Lisi, George P GP; Palermo, Giulia G
Publication Date: 2021-12-15
Variant appearance in text: PC: K855A
PubMed Link:
34908530
Variant Present in the following documents:
elife-73601.pdf
View BVdb publication page