HR c.561A>G ;(p.V187=)

Variant ID: 8-21986123-T-C

NM_005144.4(HR):c.561A>G;(p.V187=)

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: HR: 561A>G
PubMed Link: 29973717
Variant Present in the following documents:
  • Main text
  • emss-78070.pdf
View BVdb publication page