NOTCH1 c.1720C>T ;(p.P574S)

Variant ID: 9-139410118-G-A

NM_017617.3(NOTCH1):c.1720C>T;(p.P574S)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: NOTCH1: P574S
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2
View BVdb publication page



A clinically annotated post-mortem approach to study multi-organ somatic mutational clonality in normal tissues.

Scientific Reports
Luijts, Tom T; Elliott, Kerryn K; Siaw, Joachim Tetteh JT; Van de Velde, Joris J; Beyls, Elien E; Claeys, Arne A; Lammens, Tim T; Larsson, Erik E; Willaert, Wouter W; Vral, Anne A; Van den Eynden, Jimmy J
Publication Date: 2022-06-20

Variant appearance in text: NOTCH1: P574S
PubMed Link: 35725896
Variant Present in the following documents:
  • 41598_2022_14240_MOESM2_ESM.xls, sheet 2
View BVdb publication page



Deep sequencing as a probe of normal stem cell fate and preneoplasia in human epidermis.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Simons, Benjamin D BD
Publication Date: 2016-01-05

Variant appearance in text: NOTCH1: P574S
PubMed Link: 26699486
Variant Present in the following documents:
  • Main text
View BVdb publication page