SI c.1562A>C ;(p.N521T)

Variant ID: 3-164767614-T-G

NM_001041.3(SI):c.1562A>C;(p.N521T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Defects in 8-oxo-guanine repair pathway cause high frequency of C > A substitutions in neuroblastoma.

Proceedings Of The National Academy Of Sciences Of The United States Of America
van den Boogaard, Marlinde L ML; Oka, Rurika R; Hakkert, Anne A; Schild, Linda L; Ebus, Marli E ME; van Gerven, Michael R MR; Zwijnenburg, Danny A DA; Molenaar, Piet P; Hoyng, Lieke L LL; Dolman, M Emmy M MEM; Essing, Anke H W AHW; Koopmans, Bianca B; Helleday, Thomas T; Drost, Jarno J; van Boxtel, Ruben R; Versteeg, Rogier R; Koster, Jan J; Molenaar, Jan J JJ
Publication Date: 2021-09-07

Variant appearance in text: SI: N521T
PubMed Link: 34479993
Variant Present in the following documents:
  • pnas.2007898118.sapp.pdf
View BVdb publication page