SHE
Src homology 2 domain containing E
Summary
Predicted to enable phosphotyrosine residue binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs534092643 | 1:154,447,765 | C/T | — | — |
| rs7555748 | 1:154,450,919 | A/C | — | — |
| rs76095693 | 1:154,451,531 | T/C | downstream gene variant | — |
| rs375158598 | 1:154,456,635 | T/C | — | uncertain significance |
| rs2525800708 | 1:154,456,789 | T/C | — | uncertain significance |
| rs182352757 | 1:154,457,171 | G/A | regulatory region variant | — |
| rs12756266 | 1:154,457,349 | G/A | downstream gene variant | — |
| rs367732076 | 1:154,458,473 | C/G | — | uncertain significance |
| rs376993522 | 1:154,458,479 | T/C | — | uncertain significance |
| rs377637019 | 1:154,458,488 | G/A | — | uncertain significance |
| rs1692188120 | 1:154,459,043 | C/T | — | uncertain significance |
| rs766111652 | 1:154,459,088 | A/C | — | uncertain significance |
| rs142905292 | 1:154,459,138 | C/T | — | uncertain significance |
| rs1440844893 | 1:154,461,538 | C/T | — | uncertain significance |
| rs750899996 | 1:154,461,586 | G/C | — | uncertain significance |
| rs955844977 | 1:154,461,613 | C/T | — | uncertain significance |
| rs369258464 | 1:154,461,665 | G/A | — | uncertain significance |
| rs774854528 | 1:154,461,670 | T/C | — | uncertain significance |
| rs1435853354 | 1:154,461,677 | T/C | — | uncertain significance |
| rs999957410 | 1:154,461,695 | G/C | — | uncertain significance |
| rs754849767 | 1:154,461,721 | C/T | — | uncertain significance |
| rs199836449 | 1:154,461,751 | C/A | — | uncertain significance |
| rs192596341 | 1:154,468,433 | A/C | regulatory region variant | — |
| rs117103761 | 1:154,469,931 | T/A | regulatory region variant | — |
| rs770119615 | 1:154,471,671 | C/T | — | uncertain significance |
| rs188277002 | 1:154,472,340 | T/C | upstream gene variant | — |
| rs1332272611 | 1:154,473,989 | A/G | — | uncertain significance |
| rs769592829 | 1:154,474,016 | T/C | — | likely benign |
| rs747094772 | 1:154,474,154 | C/T | — | uncertain significance |
| rs1157661756 | 1:154,474,193 | A/G | — | uncertain significance |
| rs765721556 | 1:154,474,220 | C/A | — | uncertain significance |
| rs748176496 | 1:154,474,249 | G/C | — | uncertain significance |
| rs12729317 | 1:154,474,322 | C/T | — | uncertain significance |
| rs751880960 | 1:154,474,340 | G/A | — | uncertain significance |
| rs756212050 | 1:154,474,370 | A/T | — | uncertain significance |
| rs1692790282 | 1:154,474,430 | G/A | — | uncertain significance |
| rs185662597 | 1:154,474,438 | G/A | — | uncertain significance |
| rs907101218 | 1:154,474,445 | C/T | — | uncertain significance |
| rs965660691 | 1:154,474,478 | C/G | — | uncertain significance |
| rs577298426 | 1:154,474,487 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.