Profile Response Detail


Missing content? – Request curation!

Request curation for specific Genes, variants, or PubMed publications.

Have questions, comments or suggestions? - Let us know!

Email us at :

Molecular Profile ASXL1 inact mut
Therapy N/A
Indication/Tumor Type myelodysplastic/myeloproliferative neoplasm
Response Type not applicable


  • Case insensitive filtering will display rows where any text in any cell matches the filter term
  • Simple literal full or partial string matches
  • Separate multiple filter terms with a spaces, order doesn't matter (a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page, filtering has no impact on query parameters
  • Use quotes to match a longer phrase which contains spaces "mtor c1483f"


  • Generally, the default sort order for tables is set to be first column ascending, however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column, be sure to set ascending or descending order for a given column, before moving on to the next column.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
ASXL1 inact mut myelodysplastic/myeloproliferative neoplasm not applicable N/A Clinical Study Prognostic In multiple clinical studies, nonsense and frameshift mutations in ASXL1 were associated with decreased overall survival in patients with chronic myelomonocytic leukemia (PMID: 26849014, PMID: 23690417, PMID: 20880116). 20880116 26849014 23690417
PubMed Id Reference Title Details
(20880116) ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia. Full reference...
(26849014) Cytogenetic and molecular abnormalities in chronic myelomonocytic leukemia. Full reference...
(23690417) Prognostic score including gene mutations in chronic myelomonocytic leukemia. Full reference...