RBM15
RNA binding motif protein 15
Summary
Members of the SPEN (Split-end) family of proteins, including RBM15, have repressor function in several signaling pathways and may bind to RNA through interaction with spliceosome components (Hiriart et al., 2005 [PubMed 16129689]).[supplied by OMIM, Feb 2009]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs779015876 | 1:110,882,056 | C/T | — | uncertain significance |
| rs147573730 | 1:110,882,059 | G/A | — | uncertain significance |
| rs760086929 | 1:110,882,076 | C/T | — | uncertain significance |
| rs1323639524 | 1:110,882,088 | C/T | — | uncertain significance |
| rs750584732 | 1:110,882,092 | T/A | — | uncertain significance |
| rs2525001804 | 1:110,882,100 | A/G | — | uncertain significance |
| rs1357994083 | 1:110,882,101 | C/G | — | uncertain significance |
| rs201292259 | 1:110,882,116 | G/A | — | uncertain significance |
| rs1256017992 | 1:110,882,131 | G/A | — | uncertain significance |
| rs368721808 | 1:110,882,184 | G/C | — | uncertain significance |
| rs199528701 | 1:110,882,272 | G/A | missense variant | — |
| rs781645412 | 1:110,882,453 | C/G | — | uncertain significance |
| rs1271095060 | 1:110,882,485 | C/T | — | uncertain significance |
| rs200933258 | 1:110,882,499 | T/G | — | uncertain significance |
| rs60454212 | 1:110,882,513 | C/T | — | benign |
| rs1384760735 | 1:110,882,736 | C/T | — | uncertain significance |
| rs768241522 | 1:110,882,790 | C/T | — | uncertain significance |
| rs200277475 | 1:110,882,826 | C/T | — | uncertain significance |
| rs139719642 | 1:110,882,830 | C/T | — | uncertain significance |
| rs768296558 | 1:110,882,871 | C/T | — | uncertain significance |
| rs763275756 | 1:110,883,017 | A/C | — | uncertain significance |
| rs139024479 | 1:110,883,096 | C/T | — | uncertain significance |
| rs1166283363 | 1:110,883,339 | A/G | — | uncertain significance |
| rs1179366059 | 1:110,883,382 | C/T | — | uncertain significance |
| rs61740988 | 1:110,883,644 | G/A | — | benign |
| rs144499925 | 1:110,883,697 | C/T | — | likely benign |
| rs758837325 | 1:110,883,724 | A/G | — | uncertain significance |
| rs2523875040 | 1:110,883,765 | C/G | — | uncertain significance |
| rs761567136 | 1:110,883,792 | C/T | — | uncertain significance |
| rs773151139 | 1:110,883,802 | C/T | — | uncertain significance |
| rs2523876526 | 1:110,883,844 | C/G | — | uncertain significance |
| rs780243194 | 1:110,883,867 | C/G | — | uncertain significance |
| rs1553224979 | 1:110,883,939 | C/A | — | other |
| rs375287873 | 1:110,884,087 | A/G | — | uncertain significance |
| rs1183004190 | 1:110,884,099 | C/T | — | uncertain significance |
| rs773829825 | 1:110,884,110 | C/T | — | uncertain significance |
| rs1309272381 | 1:110,884,162 | G/A | — | uncertain significance |
| rs2523879584 | 1:110,884,224 | A/G | — | uncertain significance |
| rs767879552 | 1:110,884,400 | G/T | — | uncertain significance |
| rs61745292 | 1:110,884,493 | T/C | — | benign |
| rs375892527 | 1:110,884,501 | A/C | — | uncertain significance |
| rs2523881465 | 1:110,884,579 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.