TP53 c.658_663del ;(p.Y220_E221del)

Variant ID: 17-7578186-GCTCATA-G

NM_000546.5(TP53):c.658_663del;(p.Y220_E221del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions.

Nature
Zimmermann, Michal M; Murina, Olga O; Reijns, Martin A M MAM; Agathanggelou, Angelo A; Challis, Rachel R; Tarnauskaitė, Žygimantė Ž; Muir, Morwenna M; Fluteau, Adeline A; Aregger, Michael M; McEwan, Andrea A; Yuan, Wei W; Clarke, Matthew M; Lambros, Maryou B MB; Paneesha, Shankara S; Moss, Paul P; Chandrashekhar, Megha M; Angers, Stephane S; Moffat, Jason J; Brunton, Valerie G VG; Hart, Traver T; de Bono, Johann J; Stankovic, Tatjana T; Jackson, Andrew P AP; Durocher, Daniel D
Publication Date: 2018-07

Variant appearance in text: TP53: 658_663del
PubMed Link: 29973717
Variant Present in the following documents:
  • Main text
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