MPHOSPH10
M-phase phosphoprotein 10
Summary
This gene encodes a protein that is phosphorylated during mitosis. The protein localizes to the nucleolus during interphase and to the chromosomes during M phase. The protein associates with the U3 small nucleolar ribonucleoprotein 60-80S complexes and may be involved in pre-rRNA processing. [provided by RefSeq, Dec 2010]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778717737 | 2:71,357,800 | C/A | — | uncertain significance |
| rs770141068 | 2:71,357,881 | T/A | — | uncertain significance |
| rs138723053 | 2:71,360,060 | C/A | — | benign |
| rs1437832474 | 2:71,360,083 | T/C | — | uncertain significance |
| rs780619664 | 2:71,360,105 | G/A | — | likely benign |
| rs141436611 | 2:71,360,281 | C/T | — | likely benign |
| rs778155378 | 2:71,360,315 | A/T | — | uncertain significance |
| rs10175940 | 2:71,360,356 | G/A | — | benign |
| rs2465938758 | 2:71,360,359 | A/T | — | likely benign |
| rs759130310 | 2:71,360,366 | A/G | — | uncertain significance |
| rs771641275 | 2:71,360,375 | C/T | — | uncertain significance |
| rs76328738 | 2:71,360,399 | A/G | — | benign |
| rs752013233 | 2:71,360,494 | G/A | — | uncertain significance |
| rs745602482 | 2:71,360,561 | C/G | — | uncertain significance |
| rs762085663 | 2:71,360,611 | G/C | — | uncertain significance |
| rs777703268 | 2:71,360,628 | G/T | — | uncertain significance |
| rs146238687 | 2:71,360,639 | T/A | — | uncertain significance |
| rs147378452 | 2:71,360,657 | T/C | — | benign |
| rs768263959 | 2:71,361,082 | G/A | — | uncertain significance |
| rs139834642 | 2:71,361,180 | A/G | — | likely benign |
| rs1361253242 | 2:71,361,211 | C/T | — | uncertain significance |
| rs139416675 | 2:71,361,223 | G/A | — | likely benign |
| rs747713675 | 2:71,361,234 | A/G | — | uncertain significance |
| rs773267079 | 2:71,361,769 | G/A | — | uncertain significance |
| rs757922970 | 2:71,361,845 | C/T | — | uncertain significance |
| rs1225671568 | 2:71,365,635 | G/A | — | uncertain significance |
| rs768234906 | 2:71,365,755 | C/T | — | uncertain significance |
| rs370917892 | 2:71,368,380 | C/T | — | uncertain significance |
| rs201469945 | 2:71,368,381 | G/A | — | uncertain significance |
| rs2465955943 | 2:71,371,589 | A/G | — | uncertain significance |
| rs2465955972 | 2:71,371,601 | A/G | — | uncertain significance |
| rs147470609 | 2:71,371,658 | T/A | — | uncertain significance |
| rs4852762 | 2:71,373,036 | C/T | intron variant | — |
| rs773869811 | 2:71,375,210 | G/T | — | uncertain significance |
| rs1313891338 | 2:71,376,358 | A/C | — | uncertain significance |
| rs765570885 | 2:71,376,396 | C/T | — | uncertain significance |
| rs539937334 | 2:71,376,420 | G/A | — | uncertain significance |
| rs771463759 | 2:71,376,470 | C/T | — | uncertain significance |
| rs115361918 | 2:71,376,471 | G/A | — | likely benign |
| rs755975815 | 2:71,376,521 | A/C | — | uncertain significance |
| rs150611026 | 2:71,376,568 | A/C | — | uncertain significance |
| rs775698142 | 2:71,377,054 | A/T | — | uncertain significance |
| rs756517390 | 2:71,377,125 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.