MLF1
myeloid leukemia factor 1
Summary
This gene encodes an oncoprotein which is thought to play a role in the phenotypic determination of hemopoetic cells. Translocations between this gene and nucleophosmin have been associated with myelodysplastic syndrome and acute myeloid leukemia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2276773 | 3:158,287,455 | A/T | — | — |
| rs62287933 | 3:158,290,565 | A/G | upstream gene variant | — |
| rs6779426 | 3:158,295,170 | C/T | intron variant | — |
| rs9844502 | 3:158,298,615 | C/A | — | — |
| rs9864508 | 3:158,298,703 | T/C | intron variant | — |
| rs368107623 | 3:158,310,248 | A/G | — | uncertain significance |
| rs754226445 | 3:158,310,255 | G/A | — | uncertain significance |
| rs143826689 | 3:158,310,353 | G/T | — | uncertain significance |
| rs371041058 | 3:158,311,175 | C/T | — | likely benign |
| rs779983108 | 3:158,311,176 | G/T | — | likely benign |
| rs747034048 | 3:158,311,208 | G/C | — | uncertain significance |
| rs35009328 | 3:158,314,689 | G/A | — | benign |
| rs1291191516 | 3:158,315,875 | C/T | — | uncertain significance |
| rs199951975 | 3:158,315,948 | C/T | — | uncertain significance |
| rs765550387 | 3:158,315,981 | G/T | — | uncertain significance |
| rs78151625 | 3:158,316,726 | T/A | — | — |
| rs73024716 | 3:158,317,821 | G/A | — | benign |
| rs78816147 | 3:158,317,949 | C/T | — | benign |
| rs375333288 | 3:158,320,593 | T/C | — | likely benign |
| rs4875 | 3:158,320,597 | T/C | — | benign |
| rs753077740 | 3:158,320,622 | T/C | — | uncertain significance |
| rs867309513 | 3:158,320,694 | C/T | — | uncertain significance |
| rs15967 | 3:158,320,703 | C/A | — | benign |
| rs200248107 | 3:158,320,712 | C/T | — | likely benign |
| rs775271526 | 3:158,322,932 | A/C | — | uncertain significance |
| rs141302132 | 3:158,322,934 | T/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.