SHD
Src homology 2 domain containing transforming protein D
Summary
Predicted to enable phosphotyrosine residue binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs766092262 | 19:4,280,077 | G/T | — | uncertain significance |
| rs1971240902 | 19:4,280,098 | G/A | — | uncertain significance |
| rs780651125 | 19:4,280,214 | C/T | — | uncertain significance |
| rs375627519 | 19:4,280,215 | G/T | — | uncertain significance |
| rs1002415225 | 19:4,280,257 | C/T | — | uncertain significance |
| rs1971243883 | 19:4,280,262 | G/C | — | uncertain significance |
| rs776043166 | 19:4,280,289 | C/T | — | uncertain significance |
| rs750115227 | 19:4,280,307 | G/T | — | uncertain significance |
| rs748832306 | 19:4,282,035 | T/C | — | — |
| rs2512646982 | 19:4,282,891 | G/C | — | uncertain significance |
| rs558716922 | 19:4,282,925 | C/T | — | uncertain significance |
| rs1169598445 | 19:4,282,930 | G/A | — | uncertain significance |
| rs1287359902 | 19:4,282,933 | G/A | — | uncertain significance |
| rs138591689 | 19:4,283,068 | G/A | — | uncertain significance |
| rs762367085 | 19:4,283,098 | C/A | — | uncertain significance |
| rs1269049964 | 19:4,283,129 | C/T | — | uncertain significance |
| rs144605369 | 19:4,283,151 | C/G | — | uncertain significance |
| rs2512647417 | 19:4,283,169 | T/A | — | uncertain significance |
| rs1769377052 | 19:4,283,170 | G/C | — | uncertain significance |
| rs1317828041 | 19:4,284,790 | G/C | — | uncertain significance |
| rs374912178 | 19:4,284,810 | C/T | — | likely benign |
| rs35264197 | 19:4,286,315 | A/G | — | — |
| rs997031004 | 19:4,288,272 | C/G | — | uncertain significance |
| rs201387982 | 19:4,290,461 | T/G | — | uncertain significance |
| rs765408203 | 19:4,290,478 | C/T | — | uncertain significance |
| rs777477718 | 19:4,290,485 | G/A | — | uncertain significance |
| rs535726961 | 19:4,290,538 | G/A | — | uncertain significance |
| rs150781210 | 19:4,290,586 | G/A | — | uncertain significance |
| rs199704298 | 19:4,290,591 | T/A | — | uncertain significance |
| rs1361094622 | 19:4,290,602 | T/C | — | uncertain significance |
| rs139133532 | 19:4,290,610 | G/A | — | uncertain significance |
| rs758005259 | 19:4,290,617 | C/T | — | uncertain significance |
| rs147445732 | 19:4,290,623 | C/A | — | uncertain significance |
| rs2512655099 | 19:4,290,626 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.