NOTCH1 c.7496_7497insTCC ;(p.S2499_H2500insP)

Variant ID: 9-139390694-G-GGGA

NM_017617.3(NOTCH1):c.7496_7497insTCC;(p.S2499_H2500insP)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Acquired somatic variants in inherited myeloid malignancies.

Leukemia
Armes, Hannah H; Rio-Machin, Ana A; Krizsán, Szilvia S; Bödör, Csaba C; Kaya, Fadimana F; Bewicke-Copley, Findlay F; Alnajar, Jenna J; Walne, Amanda A; Péterffy, Borbála B; Tummala, Hemanth H; Rouault-Pierre, Kevin K; Dokal, Inderjeet I; Vulliamy, Tom T; Fitzgibbon, Jude J
Publication Date: 2022-05

Variant appearance in text: NOTCH1: 7496_7497insTCC
PubMed Link: 35140362
Variant Present in the following documents:
  • 41375_2022_1515_MOESM3_ESM.xlsx, sheet 1
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