TRIP13
thyroid hormone receptor interactor 13
Summary
This gene encodes a protein that interacts with thyroid hormone receptors, also known as hormone-dependent transcription factors. The gene product interacts specifically with the ligand binding domain. This gene is one of several that may play a role in early-stage non-small cell lung cancer. [provided by RefSeq, Oct 2009]
Known Variants101 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs542129307 | 5:892,837 | C/T | — | benign |
| rs111286164 | 5:892,846 | C/T | — | benign |
| rs149969411 | 5:892,869 | G/A | — | benign |
| rs113990338 | 5:892,955 | G/A | — | benign |
| rs375328821 | 5:893,164 | G/A | — | likely benign |
| rs780778324 | 5:893,190 | A/G | — | conflicting classifications of pathogenicity |
| rs369670075 | 5:893,195 | C/A | — | uncertain significance |
| rs948268218 | 5:893,211 | C/G | — | uncertain significance |
| rs201469092 | 5:893,216 | C/A | — | likely benign |
| rs184436527 | 5:893,221 | C/T | — | benign |
| rs752105824 | 5:893,222 | C/T | — | likely benign |
| rs13181961 | 5:893,356 | C/G | — | benign |
| rs75110591 | 5:893,425 | C/G | — | benign |
| rs1252521225 | 5:894,932 | T/C | — | likely benign |
| rs758258842 | 5:895,032 | A/G | — | uncertain significance |
| rs1804865 | 5:895,053 | G/A | — | uncertain significance |
| rs28672176 | 5:896,544 | C/T | — | benign |
| rs7730877 | 5:896,657 | G/T | — | benign |
| rs7708206 | 5:896,726 | C/G | — | benign |
| rs762063056 | 5:896,785 | C/T | — | uncertain significance |
| rs769362210 | 5:896,796 | C/A | — | uncertain significance |
| rs144634558 | 5:896,798 | T/C | — | benign |
| rs144812796 | 5:896,869 | A/G | — | likely benign |
| rs920980 | 5:896,983 | A/G | — | benign |
| rs2531653169 | 5:900,641 | T/C | — | uncertain significance |
| rs1240211104 | 5:900,643 | C/T | — | likely benign |
| rs370143173 | 5:900,646 | T/C | — | likely benign |
| rs72703173 | 5:900,839 | T/C | — | benign |
| rs73734002 | 5:900,880 | C/T | — | benign |
| rs60979695 | 5:900,914 | G/A | — | benign |
| rs6878334 | 5:901,423 | T/C | — | benign |
| rs372479379 | 5:901,451 | A/G | — | likely benign |
| rs1580052277 | 5:901,521 | C/G | — | likely benign |
| rs111928171 | 5:901,527 | C/T | — | likely benign |
| rs759712974 | 5:901,529 | G/A | — | pathogenic |
| rs80338980 | 5:901,553 | T/C | — | benign |
| rs73020933 | 5:904,125 | C/T | — | benign |
| rs1754056948 | 5:904,319 | A/G | — | pathogenic |
| rs780884111 | 5:904,329 | C/T | — | uncertain significance |
| rs375068192 | 5:904,345 | G/A | — | likely benign |
| rs12518024 | 5:904,374 | G/T | — | benign |
| rs45586233 | 5:907,094 | C/T | — | benign |
| rs149881196 | 5:907,250 | G/A | — | likely benign |
| rs568450907 | 5:907,275 | C/T | — | likely benign |
| rs267600743 | 5:907,287 | C/T | — | likely benign |
| rs55900306 | 5:907,505 | G/A | — | benign |
| rs73020941 | 5:907,935 | T/A | — | benign |
| rs73734409 | 5:908,056 | C/T | — | benign |
| rs376089662 | 5:908,096 | G/A | — | likely benign |
| rs1131692330 | 5:908,102 | G/C | — | pathogenic |
| rs769856470 | 5:908,142 | G/A | — | uncertain significance |
| rs2531664282 | 5:908,151 | G/A | — | uncertain significance |
| rs749293094 | 5:908,153 | T/C | — | likely benign |
| rs183763272 | 5:908,162 | C/T | — | benign |
| rs1203102465 | 5:908,169 | G/A | — | pathogenic |
| rs761215009 | 5:908,177 | G/A | — | likely benign |
| rs2531664455 | 5:908,190 | G/T | — | uncertain significance |
| rs141364266 | 5:908,206 | A/G | — | benign |
| rs140220222 | 5:908,487 | C/T | — | likely benign |
| rs762906422 | 5:908,488 | G/A | — | uncertain significance |
| rs143998019 | 5:908,508 | G/A | — | likely benign |
| rs367951777 | 5:908,514 | C/T | — | likely benign |
| rs146441673 | 5:908,535 | C/T | — | likely benign |
| rs72703185 | 5:908,588 | A/G | — | benign |
| rs79236992 | 5:908,590 | G/A | — | benign |
| rs41283157 | 5:908,596 | A/G | — | benign |
| rs60113694 | 5:908,649 | T/C | — | benign |
| rs77084821 | 5:911,811 | G/A | — | benign |
| rs140779385 | 5:911,997 | C/T | — | likely benign |
| rs772834014 | 5:911,998 | G/A | — | uncertain significance |
| rs201234602 | 5:912,010 | G/A | — | uncertain significance |
| rs200589704 | 5:912,070 | A/G | — | uncertain significance |
| rs1035323563 | 5:912,079 | A/G | — | uncertain significance |
| rs2531670905 | 5:912,107 | T/C | — | uncertain significance |
| rs72703193 | 5:914,309 | C/T | — | benign |
| rs72703194 | 5:914,455 | G/A | — | benign |
| rs193088237 | 5:914,560 | C/T | — | benign |
| rs951037088 | 5:914,598 | C/T | — | uncertain significance |
| rs376882637 | 5:914,619 | C/G | missense variant | uncertain significance |
| rs908695403 | 5:914,655 | G/A | — | uncertain significance |
| rs35725571 | 5:914,664 | T/C | — | benign |
| rs145170850 | 5:914,669 | C/T | — | benign |
| rs56124764 | 5:914,936 | A/G | — | benign |
| rs56315432 | 5:915,907 | T/C | — | benign |
| rs56313889 | 5:915,958 | T/C | — | benign |
| rs777202257 | 5:916,021 | A/G | — | uncertain significance |
| rs143798038 | 5:916,035 | A/G | — | likely benign |
| rs1161783357 | 5:916,087 | A/G | — | uncertain significance |
| rs749017084 | 5:916,088 | G/A | — | uncertain significance |
| rs60132887 | 5:916,890 | T/G | — | benign |
| rs1055758128 | 5:916,907 | C/G | — | benign |
| rs72703199 | 5:916,975 | G/A | — | benign |
| rs58876062 | 5:917,106 | G/C | — | benign |
| rs58157086 | 5:917,110 | G/A | — | benign |
| rs778623979 | 5:917,139 | T/C | — | uncertain significance |
| rs148312124 | 5:917,145 | G/A | — | conflicting classifications of pathogenicity |
| rs774804423 | 5:917,176 | C/T | — | likely benign |
| rs1579206280 | 5:917,188 | A/G | — | likely benign |
| rs759305318 | 5:917,191 | G/A | — | likely benign |
| rs200263887 | 5:917,213 | A/C | — | uncertain significance |
Showing 100 of 101 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.