Variant ID: 1-55518019-GGGCAGGGTCA-G

NM_174936.3(PCSK9):c.592_601del;(p.G198Wfs*66)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Recurrent deletions in clonal hematopoiesis are driven by microhomology-mediated end joining.

Nature Communications
Feldman, Tzah T; Bercovich, Akhiad A; Moskovitz, Yoni Y; Chapal-Ilani, Noa N; Mitchell, Amanda A; Medeiros, Jessie J F JJF; Biezuner, Tamir T; Kaushansky, Nathali N; Minden, Mark D MD; Gupta, Vikas V; Milyavsky, Michael M; Livneh, Zvi Z; Tanay, Amos A; Shlush, Liran I LI
Publication Date: 2021-04-28

Variant appearance in text: PCSK9: 592_601del
PubMed Link: 33911081
Variant Present in the following documents:
  • 41467_2021_22803_MOESM4_ESM.xlsx
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