RUNX2 c.693A>C ;(p.R231S)

Variant ID: 6-45459685-A-C

NM_001024630.3(RUNX2):c.693A>C;(p.R231S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes.

Npj Precision Oncology
Ritch, Elie J EJ; Herberts, Cameron C; Warner, Evan W EW; Ng, Sarah W S SWS; Kwan, Edmond M EM; Bacon, Jack V W JVW; Bernales, Cecily Q CQ; Schönlau, Elena E; Fonseca, Nicolette M NM; Giri, Veda N VN; Maurice-Dror, Corinne C; Vandekerkhove, Gillian G; Jones, Steven J M SJM; Chi, Kim N KN; Wyatt, Alexander W AW
Publication Date: 2023-03-13

Variant appearance in text: RUNX2: R231S
PubMed Link: 36914848
Variant Present in the following documents:
  • 41698_2023_366_MOESM2_ESM.xlsx, sheet 4
View BVdb publication page



Integrase residues that determine nucleotide preferences at sites of HIV-1 integration: implications for the mechanism of target DNA binding.

Nucleic Acids Research
Serrao, Erik E; Krishnan, Lavanya L; Shun, Ming-Chieh MC; Li, Xiang X; Cherepanov, Peter P; Engelman, Alan A; Maertens, Goedele N GN
Publication Date: 2014-04

Variant appearance in text: CCD: R231S
PubMed Link: 24520116
Variant Present in the following documents:
  • Main text
  • gku136.pdf
View BVdb publication page