PARP1 c.1573_1574delinsCC ;(p.L525P)

Variant ID: 1-226567312-AA-GG

NM_001618.3(PARP1):c.1573_1574delinsCC;(p.L525P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutant FUS causes DNA ligation defects to inhibit oxidative damage repair in Amyotrophic Lateral Sclerosis.

Nature Communications
Wang, Haibo H; Guo, Wenting W; Mitra, Joy J; Hegde, Pavana M PM; Vandoorne, Tijs T; Eckelmann, Bradley J BJ; Mitra, Sankar S; Tomkinson, Alan E AE; Van Den Bosch, Ludo L; Hegde, Muralidhar L ML
Publication Date: 2018-09-11

Variant appearance in text: PARP1: L525P
PubMed Link: 30206235
Variant Present in the following documents:
  • Main text
  • 41467_2018_6111_MOESM1_ESM.pdf
  • 41467_2018_Article_6111.pdf
View BVdb publication page