TRIP10
thyroid hormone receptor interactor 10
Summary
Enables identical protein binding activity. Predicted to be involved in actin cytoskeleton organization and signal transduction. Located in nucleoplasm. Biomarker of Huntington's disease. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10410021 | 19:6,740,380 | G/T | — | — |
| rs142559634 | 19:6,743,046 | T/C | — | uncertain significance |
| rs147177089 | 19:6,743,048 | G/C | — | uncertain significance |
| rs1968969110 | 19:6,743,064 | G/A | — | uncertain significance |
| rs377574912 | 19:6,743,069 | C/T | — | uncertain significance |
| rs774458826 | 19:6,743,223 | C/G | — | uncertain significance |
| rs140367724 | 19:6,743,224 | G/A | — | uncertain significance |
| rs985929707 | 19:6,743,247 | G/T | — | uncertain significance |
| rs2512353556 | 19:6,743,248 | G/A | — | uncertain significance |
| rs34329946 | 19:6,743,256 | C/G | — | uncertain significance |
| rs144976733 | 19:6,743,511 | C/G | — | uncertain significance |
| rs145688036 | 19:6,743,565 | C/T | — | uncertain significance |
| rs1287022392 | 19:6,743,578 | A/G | — | uncertain significance |
| rs137899128 | 19:6,743,743 | A/G | — | uncertain significance |
| rs756625759 | 19:6,743,845 | G/A | — | uncertain significance |
| rs750221894 | 19:6,744,579 | G/A | — | uncertain significance |
| rs906690475 | 19:6,744,619 | C/T | — | uncertain significance |
| rs759200847 | 19:6,744,674 | G/A | — | uncertain significance |
| rs778897347 | 19:6,744,820 | G/A | — | uncertain significance |
| rs775226645 | 19:6,744,827 | T/C | — | uncertain significance |
| rs140370711 | 19:6,744,865 | G/A | — | uncertain significance |
| rs902157922 | 19:6,744,902 | C/T | — | likely benign |
| rs200145903 | 19:6,744,932 | C/T | — | uncertain significance |
| rs920707723 | 19:6,744,964 | C/T | — | uncertain significance |
| rs749868588 | 19:6,744,965 | G/A | — | uncertain significance |
| rs932047899 | 19:6,744,971 | G/T | — | uncertain significance |
| rs767941294 | 19:6,744,979 | C/T | — | uncertain significance |
| rs142688804 | 19:6,746,475 | G/A | — | uncertain significance |
| rs756396774 | 19:6,746,515 | G/A | — | uncertain significance |
| rs201134453 | 19:6,746,539 | G/A | — | uncertain significance |
| rs1599569157 | 19:6,749,998 | A/T | — | uncertain significance |
| rs140822183 | 19:6,750,006 | A/G | — | uncertain significance |
| rs377577075 | 19:6,750,039 | A/G | — | uncertain significance |
| rs146733712 | 19:6,750,059 | G/C | — | uncertain significance |
| rs755067249 | 19:6,750,067 | A/G | — | uncertain significance |
| rs767634125 | 19:6,750,304 | C/T | — | uncertain significance |
| rs1969248147 | 19:6,750,322 | A/T | — | uncertain significance |
| rs200944790 | 19:6,750,328 | G/A | — | uncertain significance |
| rs766706299 | 19:6,750,361 | G/A | — | uncertain significance |
| rs141275848 | 19:6,750,369 | C/T | — | uncertain significance |
| rs200262718 | 19:6,750,370 | G/A | — | uncertain significance |
| rs758143129 | 19:6,750,378 | G/A | — | uncertain significance |
| rs144118150 | 19:6,750,530 | G/C | — | uncertain significance |
| rs780056390 | 19:6,751,125 | T/C | — | uncertain significance |
| rs1310163899 | 19:6,751,154 | C/T | — | uncertain significance |
| rs753953444 | 19:6,751,212 | C/T | — | uncertain significance |
| rs1049229 | 19:6,751,279 | A/G | — | benign |
| rs1049230 | 19:6,751,281 | C/T | — | benign |
| rs1049232 | 19:6,751,293 | T/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.