APOB c.2629C>G ;(p.P877A)

Variant ID: 2-21245890-G-C

NM_000384.2(APOB):c.2629C>G;(p.P877A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Germline deletion of ETV6 in familial acute lymphoblastic leukemia.

Blood Advances
Rampersaud, Evadnie E; Ziegler, David S DS; Iacobucci, Ilaria I; Payne-Turner, Debbie D; Churchman, Michelle L ML; Schrader, Kasmintan A KA; Joseph, Vijai V; Offit, Kenneth K; Tucker, Katherine K; Sutton, Rosemary R; Warby, Meera M; Chenevix-Trench, Georgia G; Huntsman, David G DG; Tsoli, Maria M; Mead, R Scott RS; Qu, Chunxu C; Leventaki, Vasiliki V; Wu, Gang G; Mullighan, Charles G CG
Publication Date: 2019-04-09

Variant appearance in text: APOB: P877A
PubMed Link: 30940639
Variant Present in the following documents:
  • Main text
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