TIGD5
tigger transposable element derived 5
Summary
The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs964458641 | 8:144,680,102 | C/A | — | uncertain significance |
| rs1268855878 | 8:144,680,116 | G/A | — | uncertain significance |
| rs2538334030 | 8:144,680,168 | C/T | — | uncertain significance |
| rs941328379 | 8:144,680,182 | C/T | — | uncertain significance |
| rs895704615 | 8:144,680,210 | T/C | — | uncertain significance |
| rs1438354402 | 8:144,680,476 | C/G | — | uncertain significance |
| rs1245883980 | 8:144,680,480 | G/T | — | uncertain significance |
| rs1829142948 | 8:144,680,544 | G/C | — | uncertain significance |
| rs1001156173 | 8:144,680,683 | A/G | — | uncertain significance |
| rs2538353019 | 8:144,680,687 | A/G | — | uncertain significance |
| rs959339122 | 8:144,680,732 | C/G | — | uncertain significance |
| rs917960294 | 8:144,680,735 | C/T | — | uncertain significance |
| rs2131381427 | 8:144,680,756 | A/C | — | uncertain significance |
| rs2538357550 | 8:144,680,797 | A/G | — | uncertain significance |
| rs2538357900 | 8:144,680,809 | T/A | — | uncertain significance |
| rs1449782639 | 8:144,680,855 | C/A | — | uncertain significance |
| rs1829167702 | 8:144,680,945 | C/G | — | uncertain significance |
| rs761667721 | 8:144,680,990 | A/G | — | uncertain significance |
| rs978222542 | 8:144,681,118 | C/G | — | uncertain significance |
| rs757796094 | 8:144,681,150 | C/A | — | uncertain significance |
| rs2538377447 | 8:144,681,366 | C/T | — | likely benign |
| rs1273779432 | 8:144,681,382 | G/T | — | uncertain significance |
| rs1186580701 | 8:144,681,392 | G/T | — | uncertain significance |
| rs149895370 | 8:144,681,397 | A/G | — | likely benign |
| rs1395750608 | 8:144,681,409 | C/G | — | uncertain significance |
| rs1199628900 | 8:144,681,433 | C/T | — | uncertain significance |
| rs370572958 | 8:144,681,482 | C/T | — | uncertain significance |
| rs377656208 | 8:144,681,505 | C/G | — | uncertain significance |
| rs2538382522 | 8:144,681,546 | G/T | — | uncertain significance |
| rs765576389 | 8:144,681,593 | G/A | — | uncertain significance |
| rs958365425 | 8:144,681,602 | T/C | — | uncertain significance |
| rs1023322197 | 8:144,681,692 | G/A | — | uncertain significance |
| rs746612378 | 8:144,681,752 | C/T | — | uncertain significance |
| rs774861731 | 8:144,681,779 | G/A | — | uncertain significance |
| rs574399245 | 8:144,681,782 | G/T | — | uncertain significance |
| rs556876276 | 8:144,681,805 | A/T | — | uncertain significance |
| rs1388569378 | 8:144,681,860 | A/C | — | uncertain significance |
| rs779921060 | 8:144,681,919 | G/T | — | uncertain significance |
| rs771134406 | 8:144,681,950 | G/A | — | uncertain significance |
| rs10094377 | 8:144,684,150 | T/C | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.