OIT3
oncoprotein induced transcript 3
Summary
This gene was identified due to its downregulation in hepatocarcinomas. The encoded protein may be involved in liver development and function. [provided by RefSeq, Sep 2016]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2492530875 | 10:74,653,560 | C/T | — | uncertain significance |
| rs1845850471 | 10:74,653,563 | C/T | — | uncertain significance |
| rs374979283 | 10:74,653,605 | G/A | — | uncertain significance |
| rs145779704 | 10:74,653,614 | G/A | — | likely benign |
| rs1459846978 | 10:74,653,615 | T/C | — | uncertain significance |
| rs763088245 | 10:74,658,445 | A/T | — | uncertain significance |
| rs138607160 | 10:74,658,519 | C/G | — | uncertain significance |
| rs150387319 | 10:74,658,558 | G/A | — | likely benign |
| rs764527932 | 10:74,658,609 | C/G | — | uncertain significance |
| rs757795414 | 10:74,658,622 | C/A | — | uncertain significance |
| rs748117158 | 10:74,658,664 | C/T | — | uncertain significance |
| rs758617355 | 10:74,658,686 | A/G | — | uncertain significance |
| rs768944375 | 10:74,658,758 | T/G | — | uncertain significance |
| rs777881853 | 10:74,658,772 | G/A | — | uncertain significance |
| rs368819550 | 10:74,660,155 | G/A | — | uncertain significance |
| rs757267854 | 10:74,660,158 | G/A | — | uncertain significance |
| rs1215770147 | 10:74,660,192 | G/A | — | uncertain significance |
| rs142263386 | 10:74,660,199 | C/T | — | likely benign |
| rs369081761 | 10:74,660,200 | G/A | — | uncertain significance |
| rs57176252 | 10:74,662,593 | C/A | intron variant | — |
| rs78295286 | 10:74,665,524 | G/T | intron variant | — |
| rs11000443 | 10:74,665,640 | C/A | intron variant | — |
| rs139396966 | 10:74,666,422 | C/T | — | uncertain significance |
| rs187484242 | 10:74,666,444 | G/A | — | uncertain significance |
| rs193095904 | 10:74,670,798 | G/A | intron variant | — |
| rs564787226 | 10:74,671,490 | A/G | — | uncertain significance |
| rs1342707538 | 10:74,671,526 | G/C | — | uncertain significance |
| rs144356620 | 10:74,671,546 | T/C | — | uncertain significance |
| rs147795814 | 10:74,671,558 | C/T | — | uncertain significance |
| rs148833304 | 10:74,671,559 | G/A | — | uncertain significance |
| rs374485108 | 10:74,671,584 | C/A | — | uncertain significance |
| rs1032850717 | 10:74,673,074 | T/G | — | uncertain significance |
| rs1355202121 | 10:74,673,102 | A/C | — | uncertain significance |
| rs2492565562 | 10:74,673,177 | C/T | — | uncertain significance |
| rs776812775 | 10:74,684,056 | G/A | — | uncertain significance |
| rs138853485 | 10:74,684,083 | C/G | — | uncertain significance |
| rs1326917550 | 10:74,684,087 | T/C | — | uncertain significance |
| rs760442286 | 10:74,684,140 | G/A | — | uncertain significance |
| rs139078371 | 10:74,684,374 | G/T | — | uncertain significance |
| rs779565370 | 10:74,684,384 | A/T | — | uncertain significance |
| rs11000452 | 10:74,688,893 | G/A | intron variant | — |
| rs921023737 | 10:74,690,367 | T/C | — | uncertain significance |
| rs755563913 | 10:74,692,160 | C/T | — | uncertain significance |
| rs370772733 | 10:74,692,161 | G/A | — | likely benign |
| rs145480078 | 10:74,692,242 | C/T | — | uncertain significance |
| rs199897742 | 10:74,692,263 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.