SRRT
serrate, RNA effector molecule
Summary
Enables mRNA cap binding complex binding activity and protein-macromolecule adaptor activity. Involved in primary miRNA processing. Located in nucleoplasm. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs111542935 | 7:100,474,185 | C/T | downstream gene variant | — |
| rs540669875 | 7:100,476,738 | G/A | — | — |
| rs775337041 | 7:100,478,992 | G/A | — | uncertain significance |
| rs1443871777 | 7:100,479,019 | G/C | — | uncertain significance |
| rs773092336 | 7:100,479,333 | G/C | — | uncertain significance |
| rs144415744 | 7:100,479,385 | C/T | — | likely benign |
| rs143241109 | 7:100,479,746 | C/T | — | benign |
| rs140854190 | 7:100,481,539 | C/T | downstream gene variant | — |
| rs145327657 | 7:100,481,718 | A/G | — | benign |
| rs201998782 | 7:100,481,743 | C/T | — | uncertain significance |
| rs769951704 | 7:100,481,744 | G/A | — | uncertain significance |
| rs2485384624 | 7:100,481,767 | A/T | — | uncertain significance |
| rs15624 | 7:100,482,026 | T/C | — | benign |
| rs775122762 | 7:100,482,028 | G/A | — | uncertain significance |
| rs780973393 | 7:100,482,148 | A/C | — | uncertain significance |
| rs139372604 | 7:100,482,165 | G/A | — | uncertain significance |
| rs1466581207 | 7:100,482,380 | A/G | — | likely benign |
| rs143173043 | 7:100,482,398 | A/C | — | uncertain significance |
| rs751698942 | 7:100,482,400 | T/G | — | uncertain significance |
| rs6942607 | 7:100,482,526 | C/G | — | benign |
| rs3757866 | 7:100,482,537 | C/T | — | benign |
| rs2485399039 | 7:100,482,551 | A/G | — | uncertain significance |
| rs773607407 | 7:100,482,563 | G/A | — | uncertain significance |
| rs780669876 | 7:100,482,636 | G/C | — | uncertain significance |
| rs149587305 | 7:100,482,649 | A/G | — | uncertain significance |
| rs150582291 | 7:100,482,918 | G/A | — | uncertain significance |
| rs753989283 | 7:100,482,986 | A/G | — | uncertain significance |
| rs888110002 | 7:100,483,356 | C/T | — | uncertain significance |
| rs144966688 | 7:100,483,932 | A/G | — | uncertain significance |
| rs149025559 | 7:100,483,945 | G/C | — | uncertain significance |
| rs149979693 | 7:100,483,963 | C/G | — | benign |
| rs147945684 | 7:100,484,043 | C/T | — | uncertain significance |
| rs12705095 | 7:100,484,381 | T/G | downstream gene variant | — |
| rs755043116 | 7:100,484,439 | C/A | — | benign |
| rs200083178 | 7:100,484,500 | G/A | — | uncertain significance |
| rs1047069689 | 7:100,484,516 | C/T | — | uncertain significance |
| rs765305318 | 7:100,484,700 | C/G | — | uncertain significance |
| rs751353837 | 7:100,484,724 | C/A | — | uncertain significance |
| rs906444936 | 7:100,484,741 | A/G | — | uncertain significance |
| rs142458683 | 7:100,484,742 | C/T | — | likely benign |
| rs1201930802 | 7:100,484,815 | G/A | — | uncertain significance |
| rs138829624 | 7:100,485,397 | C/T | — | uncertain significance |
| rs980073819 | 7:100,485,736 | G/C | — | uncertain significance |
| rs771409898 | 7:100,485,740 | C/T | — | uncertain significance |
| rs1488446928 | 7:100,485,956 | A/C | — | uncertain significance |
| rs777143598 | 7:100,485,961 | G/C | — | uncertain significance |
| rs150287642 | 7:100,486,086 | A/T | — | benign |
| rs12666989 | 7:100,486,754 | G/C | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.