SECISBP2L
SECIS binding protein 2 like
Summary
Enables RNA binding activity. Predicted to be part of ribonucleoprotein complex. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139677574 | 15:49,284,446 | T/C | — | uncertain significance |
| rs369272657 | 15:49,284,454 | G/A | — | uncertain significance |
| rs145854377 | 15:49,284,484 | T/C | — | likely benign |
| rs1210355044 | 15:49,284,580 | G/A | — | uncertain significance |
| rs953568783 | 15:49,284,604 | C/T | — | uncertain significance |
| rs778302714 | 15:49,284,616 | T/C | — | uncertain significance |
| rs2504609131 | 15:49,284,681 | T/A | — | likely benign |
| rs759467573 | 15:49,284,758 | C/T | — | uncertain significance |
| rs757799972 | 15:49,284,841 | C/T | — | uncertain significance |
| rs370194787 | 15:49,284,929 | C/T | — | uncertain significance |
| rs201669301 | 15:49,284,950 | T/C | — | uncertain significance |
| rs752268484 | 15:49,285,123 | T/C | — | uncertain significance |
| rs4775792 | 15:49,288,078 | T/G | downstream gene variant | — |
| rs1338030076 | 15:49,288,646 | A/T | — | likely benign |
| rs774919201 | 15:49,288,659 | T/C | — | uncertain significance |
| rs2504614946 | 15:49,288,717 | C/T | — | uncertain significance |
| rs150175110 | 15:49,288,727 | A/G | — | likely benign |
| rs1018039869 | 15:49,293,117 | C/G | — | uncertain significance |
| rs775385932 | 15:49,293,226 | C/G | — | uncertain significance |
| rs1220002903 | 15:49,301,515 | T/C | — | uncertain significance |
| rs1902388720 | 15:49,301,555 | T/C | — | uncertain significance |
| rs202130309 | 15:49,303,958 | C/T | — | uncertain significance |
| rs2504634162 | 15:49,303,978 | A/G | — | uncertain significance |
| rs768647046 | 15:49,304,939 | G/A | — | uncertain significance |
| rs781422387 | 15:49,304,946 | A/C | — | uncertain significance |
| rs2504635728 | 15:49,304,950 | C/A | — | uncertain significance |
| rs1902463488 | 15:49,305,006 | C/T | — | uncertain significance |
| rs1718562245 | 15:49,308,778 | T/G | — | uncertain significance |
| rs1555386151 | 15:49,308,866 | A/T | — | uncertain significance |
| rs776396766 | 15:49,308,889 | A/T | — | uncertain significance |
| rs1037656007 | 15:49,311,644 | C/T | — | uncertain significance |
| rs1432890591 | 15:49,311,676 | T/C | — | uncertain significance |
| rs545970053 | 15:49,311,682 | T/A | — | uncertain significance |
| rs753115128 | 15:49,311,733 | C/T | — | uncertain significance |
| rs1902767787 | 15:49,319,657 | C/T | — | uncertain significance |
| rs752482865 | 15:49,320,653 | C/A | — | likely benign |
| rs753873715 | 15:49,320,655 | T/C | — | uncertain significance |
| rs1215873949 | 15:49,320,703 | T/G | — | uncertain significance |
| rs556587603 | 15:49,320,796 | C/A | — | uncertain significance |
| rs371138651 | 15:49,320,862 | C/T | — | uncertain significance |
| rs2504656769 | 15:49,320,874 | G/T | — | uncertain significance |
| rs200133351 | 15:49,325,225 | T/C | — | uncertain significance |
| rs370394016 | 15:49,325,245 | A/C | — | uncertain significance |
| rs747877371 | 15:49,325,246 | C/A | — | uncertain significance |
| rs149913295 | 15:49,325,267 | T/G | — | uncertain significance |
| rs1902930711 | 15:49,325,275 | A/G | — | uncertain significance |
| rs2504661928 | 15:49,325,282 | G/T | — | uncertain significance |
| rs2504664725 | 15:49,327,559 | T/C | — | uncertain significance |
| rs770867762 | 15:49,327,575 | T/C | — | uncertain significance |
| rs138614543 | 15:49,327,610 | C/T | — | uncertain significance |
| rs111675861 | 15:49,327,680 | G/C | — | uncertain significance |
| rs774060686 | 15:49,327,749 | T/C | — | uncertain significance |
| rs769057229 | 15:49,329,805 | C/G | — | uncertain significance |
| rs1595796980 | 15:49,329,843 | T/C | — | uncertain significance |
| rs559985240 | 15:49,329,893 | A/T | — | uncertain significance |
| rs200335700 | 15:49,329,894 | T/C | — | uncertain significance |
| rs1156440145 | 15:49,329,912 | C/G | — | uncertain significance |
| rs748698445 | 15:49,329,914 | G/A | — | uncertain significance |
| rs11634901 | 15:49,335,218 | C/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.