TNS4
tensin 4
Summary
Predicted to enable actin binding activity. Involved in protein localization. Located in cytosol and focal adhesion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs188409544 | 17:38,632,094 | A/G | regulatory region variant | — |
| rs762008294 | 17:38,633,919 | G/A | — | uncertain significance |
| rs968469515 | 17:38,633,956 | G/C | — | uncertain significance |
| rs2544467241 | 17:38,634,562 | G/A | — | uncertain significance |
| rs750175359 | 17:38,634,584 | A/T | — | uncertain significance |
| rs145753216 | 17:38,634,835 | C/T | — | uncertain significance |
| rs1402725575 | 17:38,634,890 | G/A | — | uncertain significance |
| rs372307680 | 17:38,635,989 | G/A | — | uncertain significance |
| rs138638819 | 17:38,636,035 | C/T | — | uncertain significance |
| rs956137923 | 17:38,636,047 | C/T | — | uncertain significance |
| rs2035897760 | 17:38,636,058 | T/C | — | uncertain significance |
| rs140032692 | 17:38,636,954 | G/A | — | benign |
| rs1340374224 | 17:38,637,006 | C/A | — | uncertain significance |
| rs2035911703 | 17:38,637,011 | C/T | — | uncertain significance |
| rs201890192 | 17:38,638,441 | C/T | — | uncertain significance |
| rs140998686 | 17:38,638,644 | C/G | — | uncertain significance |
| rs542606977 | 17:38,640,787 | C/T | — | uncertain significance |
| rs910753533 | 17:38,640,846 | C/T | — | uncertain significance |
| rs140376684 | 17:38,641,214 | G/A | — | uncertain significance |
| rs768504850 | 17:38,641,228 | C/A | — | uncertain significance |
| rs145572558 | 17:38,641,254 | C/A | — | likely benign |
| rs2544485285 | 17:38,643,404 | G/T | — | uncertain significance |
| rs772361427 | 17:38,643,429 | G/A | — | uncertain significance |
| rs144692706 | 17:38,643,441 | C/T | — | benign |
| rs369181876 | 17:38,643,542 | G/C | — | uncertain significance |
| rs142505472 | 17:38,644,861 | C/T | — | uncertain significance |
| rs371709466 | 17:38,644,915 | G/A | — | uncertain significance |
| rs148373689 | 17:38,644,939 | G/A | — | likely benign |
| rs2544489030 | 17:38,644,976 | G/A | — | uncertain significance |
| rs745659131 | 17:38,645,033 | C/G | — | uncertain significance |
| rs2544489620 | 17:38,645,113 | C/G | — | uncertain significance |
| rs369999773 | 17:38,645,122 | C/T | — | uncertain significance |
| rs372422215 | 17:38,645,132 | C/T | — | uncertain significance |
| rs141593050 | 17:38,645,195 | C/T | — | likely benign |
| rs768951694 | 17:38,645,218 | A/T | — | uncertain significance |
| rs1483189613 | 17:38,645,221 | T/G | — | uncertain significance |
| rs1901187 | 17:38,646,147 | T/A | — | — |
| rs151169359 | 17:38,649,102 | G/T | intron variant | — |
| rs764944090 | 17:38,652,250 | G/A | — | uncertain significance |
| rs2544500915 | 17:38,652,347 | C/G | — | uncertain significance |
| rs763933387 | 17:38,652,385 | A/G | — | uncertain significance |
| rs2544501084 | 17:38,652,407 | G/A | — | uncertain significance |
| rs1050327322 | 17:38,652,413 | C/T | — | uncertain significance |
| rs2544501144 | 17:38,652,419 | C/G | — | uncertain significance |
| rs753848525 | 17:38,652,436 | G/A | — | uncertain significance |
| rs778971964 | 17:38,652,445 | C/G | — | uncertain significance |
| rs764518388 | 17:38,652,487 | C/T | — | likely benign |
| rs2544501616 | 17:38,652,526 | T/C | — | uncertain significance |
| rs758545542 | 17:38,652,544 | G/A | — | uncertain significance |
| rs147520841 | 17:38,652,605 | T/C | — | uncertain significance |
| rs588305 | 17:38,657,135 | G/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.