Gene | SF1 |
Variant | any |
Transcript ID (GRCh37/hg19) | ENST00000377387 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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SF1 is a member of the spliceosome machinery and missense mutations have been described in approximately 1% of myeloid neoplasms including myelodysplasia, acute myeloid leukemia and myeloproliferative neoplasms.