SEMA4D
semaphorin 4D
Summary
Enables identical protein binding activity; semaphorin receptor binding activity; and transmembrane signaling receptor activity. Involved in several processes, including positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; regulation of neuron projection development; and regulation of primary metabolic process. Located in microtubule organizing center; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants99 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13295305 | 9:91,978,397 | C/T | — | benign |
| rs200510870 | 9:91,978,764 | G/A | — | likely benign |
| rs45515192 | 9:91,978,783 | G/A | — | benign |
| rs139924853 | 9:91,991,853 | C/A | — | benign |
| rs202211452 | 9:91,991,867 | G/A | — | likely benign |
| rs73654771 | 9:91,993,615 | G/A | — | benign |
| rs2547867554 | 9:91,993,675 | G/C | — | uncertain significance |
| rs762630765 | 9:91,993,696 | C/T | — | uncertain significance |
| rs45483393 | 9:91,993,724 | T/C | — | benign |
| rs2547868630 | 9:91,993,756 | C/T | — | uncertain significance |
| rs754827390 | 9:91,993,808 | G/A | — | likely benign |
| rs1291589145 | 9:91,993,813 | A/G | — | uncertain significance |
| rs1465716552 | 9:91,993,830 | A/G | — | uncertain significance |
| rs113511187 | 9:91,993,832 | C/T | — | likely benign |
| rs146623645 | 9:91,993,833 | G/A | — | uncertain significance |
| rs879523341 | 9:91,993,846 | T/C | — | uncertain significance |
| rs767889448 | 9:91,993,854 | C/T | — | uncertain significance |
| rs141440756 | 9:91,993,855 | G/A | — | likely benign |
| rs138397887 | 9:91,994,003 | G/A | — | likely benign |
| rs374118848 | 9:91,994,007 | C/T | — | uncertain significance |
| rs79522330 | 9:91,994,026 | G/A | — | benign |
| rs62638726 | 9:91,994,101 | A/G | — | benign |
| rs200127158 | 9:91,994,149 | C/T | — | uncertain significance |
| rs139712248 | 9:91,994,157 | G/A | — | uncertain significance |
| rs149375386 | 9:91,994,158 | T/C | — | uncertain significance |
| rs201398393 | 9:91,994,199 | G/A | — | uncertain significance |
| rs1836470951 | 9:91,994,238 | G/T | — | uncertain significance |
| rs1483956796 | 9:91,994,274 | T/C | — | uncertain significance |
| rs1049353977 | 9:91,994,351 | A/C | — | uncertain significance |
| rs45464494 | 9:91,994,433 | T/C | — | benign |
| rs749016931 | 9:91,994,457 | C/T | — | likely benign |
| rs147086169 | 9:91,994,524 | G/A | — | benign |
| rs199707488 | 9:91,996,096 | G/A | — | uncertain significance |
| rs762945622 | 9:91,996,111 | G/A | — | uncertain significance |
| rs62638723 | 9:91,996,114 | G/C | — | benign |
| rs145920058 | 9:91,996,120 | C/T | — | likely benign |
| rs138859126 | 9:91,996,127 | C/T | — | likely benign |
| rs746191711 | 9:91,996,133 | G/T | — | likely benign |
| rs758081681 | 9:91,996,137 | G/A | — | uncertain significance |
| rs148298809 | 9:91,996,196 | C/T | — | likely benign |
| rs758940892 | 9:91,996,212 | G/A | — | uncertain significance |
| rs1239708763 | 9:91,996,250 | A/C | — | uncertain significance |
| rs150828049 | 9:92,001,303 | G/A | — | likely benign |
| rs772201723 | 9:92,001,316 | T/C | — | uncertain significance |
| rs201097053 | 9:92,001,320 | A/G | — | uncertain significance |
| rs770934477 | 9:92,001,359 | C/T | — | uncertain significance |
| rs73484027 | 9:92,002,292 | G/A | — | benign |
| rs575209730 | 9:92,002,356 | C/T | — | likely benign |
| rs542114524 | 9:92,002,361 | C/T | — | uncertain significance |
| rs140150679 | 9:92,002,381 | T/A | — | uncertain significance |
| rs770952167 | 9:92,002,415 | G/T | — | uncertain significance |
| rs758668973 | 9:92,002,462 | G/A | — | uncertain significance |
| rs374901596 | 9:92,002,505 | G/A | — | uncertain significance |
| rs751235986 | 9:92,003,564 | G/A | — | uncertain significance |
| rs2548032551 | 9:92,003,566 | C/A | — | uncertain significance |
| rs534671276 | 9:92,003,588 | C/T | — | uncertain significance |
| rs150937324 | 9:92,003,653 | C/G | — | likely benign |
| rs11526468 | 9:92,003,679 | C/T | missense variant | benign |
| rs117909186 | 9:92,003,689 | C/T | — | benign |
| rs768833619 | 9:92,003,700 | C/T | — | uncertain significance |
| rs557575285 | 9:92,003,711 | G/C | — | likely benign |
| rs147822490 | 9:92,003,793 | G/A | — | uncertain significance |
| rs2548037947 | 9:92,003,800 | A/G | — | uncertain significance |
| rs770018702 | 9:92,003,846 | G/A | — | likely benign |
| rs758200365 | 9:92,003,940 | G/A | — | uncertain significance |
| rs2548041456 | 9:92,003,956 | G/C | — | uncertain significance |
| rs1198553854 | 9:92,006,207 | A/T | — | uncertain significance |
| rs143643219 | 9:92,006,211 | C/A | — | benign |
| rs28377168 | 9:92,006,275 | G/A | — | benign |
| rs200460697 | 9:92,006,280 | C/T | — | uncertain significance |
| rs116833424 | 9:92,006,281 | G/A | — | benign |
| rs138867489 | 9:92,006,300 | C/T | — | uncertain significance |
| rs776161783 | 9:92,006,301 | G/A | — | uncertain significance |
| rs62638727 | 9:92,006,308 | G/A | — | benign |
| rs13287803 | 9:92,006,536 | C/A | — | — |
| rs150882263 | 9:92,007,351 | G/A | — | likely benign |
| rs781582499 | 9:92,007,377 | T/C | — | uncertain significance |
| rs374144974 | 9:92,007,450 | A/G | — | likely benign |
| rs1258698767 | 9:92,011,701 | G/C | — | uncertain significance |
| rs4877080 | 9:92,013,728 | T/G | — | — |
| rs2548197638 | 9:92,014,222 | G/C | — | uncertain significance |
| rs2548197704 | 9:92,014,225 | T/G | — | uncertain significance |
| rs1841684237 | 9:92,014,238 | A/C | — | uncertain significance |
| rs374328845 | 9:92,014,256 | G/A | — | likely benign |
| rs11265904 | 9:92,014,868 | G/A | intron variant | — |
| rs41287361 | 9:92,017,733 | G/A | intron variant | — |
| rs2133638999 | 9:92,017,794 | G/A | — | uncertain significance |
| rs62620228 | 9:92,017,815 | C/T | — | uncertain significance |
| rs949621536 | 9:92,017,817 | T/C | — | uncertain significance |
| rs13284404 | 9:92,017,824 | C/A | missense variant | benign |
| rs775789290 | 9:92,017,869 | C/T | — | uncertain significance |
| rs576002602 | 9:92,017,914 | A/G | — | uncertain significance |
| rs140873372 | 9:92,020,304 | G/A | — | uncertain significance |
| rs552738329 | 9:92,020,310 | G/A | — | uncertain significance |
| rs1355384700 | 9:92,020,362 | A/C | — | uncertain significance |
| rs56339712 | 9:92,025,757 | C/T | regulatory region variant | — |
| rs4132699 | 9:92,036,427 | A/C | upstream gene variant | — |
| rs150158729 | 9:92,066,702 | G/A | downstream gene variant | — |
| rs80068415 | 9:92,093,127 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.