TP53 c.505_531del ;(p.M169_P177del)

Variant ID: 17-7578398-GGGGGCAGCGCCTCACAACCTCCGTCAT-G

NM_000546.5(TP53):c.505_531del;(p.M169_P177del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).

Clinical Lymphoma, Myeloma & Leukemia
DiNardo, Courtney D CD; Bannon, Sarah A SA; Routbort, Mark M; Franklin, Anna A; Mork, Maureen M; Armanios, Mary M; Mace, Emily M EM; Orange, Jordan S JS; Jeff-Eke, Meselle M; Churpek, Jane E JE; Takahashi, Koichi K; Jorgensen, Jeffrey L JL; Garcia-Manero, Guillermo G; Kornblau, Steve S; Bertuch, Alison A; Cheung, Hannah H; Bhalla, Kapil K; Futreal, Andrew A; Godley, Lucy A LA; Patel, Keyur P KP
Publication Date: 2016-07

Variant appearance in text: TP53: M169_P177del
PubMed Link: 27210295
Variant Present in the following documents:
  • Main text
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