BUD13
BUD13 spliceosome associated protein
Summary
Enables RNA binding activity. Involved in mRNA splicing, via spliceosome. Located in nucleoplasm. Part of U2-type precatalytic spliceosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11556024 | 11:116,619,051 | G/A | 3 prime UTR variant | — |
| rs28927680 | 11:116,619,073 | C/T | — | — |
| rs145906707 | 11:116,619,178 | C/T | 3 prime UTR variant | — |
| rs748728060 | 11:116,619,269 | G/A | — | uncertain significance |
| rs377491137 | 11:116,619,390 | A/T | — | — |
| rs77684111 | 11:116,620,129 | G/A | intron variant | — |
| rs57950207 | 11:116,620,670 | T/C | intron variant | — |
| rs17440396 | 11:116,621,770 | G/A | intron variant | — |
| rs74368849 | 11:116,622,299 | G/A | intron variant | — |
| rs6589564 | 11:116,624,153 | C/A | — | — |
| rs139524394 | 11:116,624,922 | C/T | intron variant | — |
| rs12421652 | 11:116,625,875 | G/A | — | — |
| rs77112220 | 11:116,626,226 | C/T | intron variant | — |
| rs11825181 | 11:116,626,258 | G/A | intron variant | — |
| rs191206329 | 11:116,626,399 | C/G | intron variant | — |
| rs4938309 | 11:116,627,055 | C/A | — | — |
| rs193108398 | 11:116,627,177 | G/A | intron variant | — |
| rs756494576 | 11:116,627,900 | A/C | — | uncertain significance |
| rs2496822819 | 11:116,627,919 | G/A | — | uncertain significance |
| rs1026851262 | 11:116,627,928 | C/G | — | uncertain significance |
| rs746050926 | 11:116,627,929 | T/C | — | uncertain significance |
| rs2075295 | 11:116,628,401 | T/A | — | — |
| rs1289168813 | 11:116,628,488 | T/C | — | uncertain significance |
| rs1057036979 | 11:116,628,491 | T/C | — | uncertain significance |
| rs374136726 | 11:116,628,623 | T/C | — | likely benign |
| rs754863712 | 11:116,628,631 | T/A | — | uncertain significance |
| rs762267985 | 11:116,628,643 | T/G | — | uncertain significance |
| rs1156761722 | 11:116,628,652 | C/T | — | uncertain significance |
| rs2496826386 | 11:116,629,028 | T/C | — | uncertain significance |
| rs143244324 | 11:116,629,042 | C/A | — | uncertain significance |
| rs778142684 | 11:116,629,079 | G/A | — | uncertain significance |
| rs116588420 | 11:116,629,766 | G/T | intron variant | — |
| rs776700062 | 11:116,629,840 | C/T | — | uncertain significance |
| rs767550000 | 11:116,629,879 | G/C | — | uncertain significance |
| rs17519093 | 11:116,629,905 | G/A | intron variant | — |
| rs139212887 | 11:116,631,469 | A/T | — | uncertain significance |
| rs35004487 | 11:116,631,542 | G/C | — | benign |
| rs1403969108 | 11:116,631,615 | T/C | — | uncertain significance |
| rs139872819 | 11:116,631,912 | T/C | intron variant | — |
| rs10488699 | 11:116,632,500 | C/T | intron variant | — |
| rs11602240 | 11:116,632,798 | T/A | — | — |
| rs57641217 | 11:116,632,956 | C/T | intron variant | — |
| rs146797420 | 11:116,633,297 | A/C | — | uncertain significance |
| rs376936315 | 11:116,633,319 | T/C | — | uncertain significance |
| rs139099960 | 11:116,633,322 | C/T | — | uncertain significance |
| rs1389749849 | 11:116,633,428 | T/C | — | uncertain significance |
| rs773840463 | 11:116,633,485 | A/C | — | uncertain significance |
| rs751731755 | 11:116,633,502 | C/T | — | likely benign |
| rs759787078 | 11:116,633,503 | G/A | — | uncertain significance |
| rs1940456009 | 11:116,633,562 | G/T | — | uncertain significance |
| rs199737278 | 11:116,633,610 | C/T | — | likely benign |
| rs200542348 | 11:116,633,611 | G/A | — | uncertain significance |
| rs771442959 | 11:116,633,634 | T/C | — | uncertain significance |
| rs374148628 | 11:116,633,650 | G/A | — | uncertain significance |
| rs766417666 | 11:116,633,667 | G/A | — | likely benign |
| rs141032478 | 11:116,633,680 | T/A | — | uncertain significance |
| rs779370532 | 11:116,633,703 | G/T | — | uncertain significance |
| rs753535705 | 11:116,633,739 | G/A | — | uncertain significance |
| rs779276660 | 11:116,633,748 | T/C | — | uncertain significance |
| rs760208744 | 11:116,633,815 | G/A | — | uncertain significance |
| rs11820589 | 11:116,633,862 | G/A | missense variant | — |
| rs2540214524 | 11:116,633,871 | T/G | — | uncertain significance |
| rs12272017 | 11:116,633,874 | C/T | — | uncertain significance |
| rs2540214570 | 11:116,633,898 | G/A | — | uncertain significance |
| rs199861463 | 11:116,633,910 | C/T | — | uncertain significance |
| rs764862832 | 11:116,633,919 | C/G | — | uncertain significance |
| rs1217790444 | 11:116,633,925 | G/A | — | uncertain significance |
| rs776613811 | 11:116,633,959 | T/C | — | uncertain significance |
| rs17119975 | 11:116,634,557 | T/C | intron variant | — |
| rs2187126 | 11:116,635,784 | A/G | intron variant | — |
| rs180941480 | 11:116,636,107 | C/T | — | uncertain significance |
| rs376363328 | 11:116,636,108 | G/A | — | uncertain significance |
| rs754721916 | 11:116,636,120 | T/C | — | uncertain significance |
| rs777824861 | 11:116,636,141 | G/A | — | uncertain significance |
| rs2540216859 | 11:116,636,155 | T/C | — | uncertain significance |
| rs12294259 | 11:116,637,146 | C/T | intron variant | — |
| rs10790162 | 11:116,639,104 | A/G | intron variant | — |
| rs188925715 | 11:116,639,682 | G/A | upstream gene variant | — |
| rs622604 | 11:116,640,062 | T/C | upstream gene variant | — |
| rs610675 | 11:116,640,094 | T/A | upstream gene variant | — |
| rs6589565 | 11:116,640,237 | A/G | upstream gene variant | — |
| rs1457927531 | 11:116,640,937 | T/C | — | uncertain significance |
| rs762502775 | 11:116,643,561 | C/A | — | uncertain significance |
| rs2540223840 | 11:116,643,562 | T/G | — | uncertain significance |
| rs369075704 | 11:116,643,574 | T/C | — | uncertain significance |
| rs1251510469 | 11:116,643,586 | C/A | — | uncertain significance |
| rs1204819465 | 11:116,643,598 | G/C | — | uncertain significance |
| rs770960697 | 11:116,643,604 | C/T | — | uncertain significance |
| rs772330925 | 11:116,643,611 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.