Varaico: Literature-Extracted Genetic Variants

Gene:SAMD9L
Variant:p.F886_Y887delFs
Back to variants list

SAMD9L

NM_152703.5:p.F886_Y887delFs

Associated Papers

New SAMD9L heterozygous mutation leading to myelodysplastic syndrome and acute myeloid leukemia: A case report and review of the literature.

Monagel DA

Cancer Reports (hoboken, N.j.), 2023

SAMD9L autoinflammatory or ataxia pancytopenia disease mutations activate cell-autonomous translational repression.

Russell AJ et al.

Proceedings of the National Academy of Sciences of the United States of America, 2021

Germline SAMD9L truncation variants trigger global translational repression.

Allenspach EJ et al.

The Journal of Experimental Medicine, 2021

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."