TDRD5
tudor domain containing 5
Summary
Predicted to be involved in P granule organization; spermatid development; and transposable element silencing by piRNA-mediated DNA methylation. Predicted to be located in chromatoid body and pi-body. Predicted to be active in synapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs896902002 | 1:179,561,797 | G/A | — | uncertain significance |
| rs138668107 | 1:179,561,901 | C/T | — | uncertain significance |
| rs199604826 | 1:179,561,916 | C/G | — | uncertain significance |
| rs758414840 | 1:179,561,930 | G/A | — | uncertain significance |
| rs1427300894 | 1:179,561,968 | C/A | — | uncertain significance |
| rs763541638 | 1:179,562,672 | A/G | — | uncertain significance |
| rs376799300 | 1:179,562,706 | C/T | — | uncertain significance |
| rs2526462675 | 1:179,562,861 | T/A | — | uncertain significance |
| rs386352369 | 1:179,562,889 | T/C | — | uncertain significance |
| rs752790470 | 1:179,562,936 | A/G | — | uncertain significance |
| rs750848742 | 1:179,564,817 | T/G | — | uncertain significance |
| rs756660429 | 1:179,564,820 | C/T | — | uncertain significance |
| rs150798452 | 1:179,564,833 | A/G | — | benign |
| rs200507631 | 1:179,564,849 | A/G | — | uncertain significance |
| rs1343188794 | 1:179,587,742 | C/A | — | uncertain significance |
| rs745509164 | 1:179,600,012 | A/C | — | uncertain significance |
| rs1338875656 | 1:179,603,643 | G/A | — | uncertain significance |
| rs2526822188 | 1:179,603,655 | C/G | — | uncertain significance |
| rs759058451 | 1:179,603,704 | A/C | — | likely benign |
| rs201849047 | 1:179,603,735 | C/T | — | uncertain significance |
| rs763278183 | 1:179,604,857 | C/T | — | uncertain significance |
| rs777262373 | 1:179,604,904 | G/C | — | uncertain significance |
| rs777050040 | 1:179,604,919 | A/G | — | likely benign |
| rs200373683 | 1:179,604,992 | A/T | — | uncertain significance |
| rs2102025801 | 1:179,609,149 | A/T | — | uncertain significance |
| rs780677767 | 1:179,609,575 | G/A | — | uncertain significance |
| rs199784694 | 1:179,620,047 | G/A | — | uncertain significance |
| rs1241099149 | 1:179,621,237 | G/T | — | uncertain significance |
| rs1447183181 | 1:179,621,296 | A/G | — | uncertain significance |
| rs2526981661 | 1:179,621,301 | C/T | — | uncertain significance |
| rs16854446 | 1:179,623,429 | A/G | — | benign |
| rs748677047 | 1:179,623,435 | A/T | — | uncertain significance |
| rs530274369 | 1:179,623,477 | G/A | — | uncertain significance |
| rs2527048643 | 1:179,631,244 | G/T | — | uncertain significance |
| rs373077224 | 1:179,631,401 | T/C | — | likely benign |
| rs73037621 | 1:179,632,503 | T/A | — | benign |
| rs375890851 | 1:179,632,553 | C/T | — | likely benign |
| rs750889576 | 1:179,632,619 | C/T | — | likely benign |
| rs147845046 | 1:179,638,333 | T/C | — | likely benign |
| rs1679727132 | 1:179,638,343 | T/G | — | likely benign |
| rs766953290 | 1:179,638,344 | G/T | — | uncertain significance |
| rs1223639736 | 1:179,638,354 | A/T | — | uncertain significance |
| rs756995942 | 1:179,638,383 | T/C | — | uncertain significance |
| rs140853709 | 1:179,638,450 | A/G | — | uncertain significance |
| rs145048355 | 1:179,638,476 | T/A | — | uncertain significance |
| rs569068618 | 1:179,656,774 | G/T | — | — |
| rs2527243452 | 1:179,659,834 | A/G | — | uncertain significance |
| rs748050482 | 1:179,659,879 | G/C | — | uncertain significance |
| rs200779614 | 1:179,659,928 | G/C | — | likely benign |
| rs984019528 | 1:179,660,056 | G/A | — | uncertain significance |
| rs369126968 | 1:179,660,069 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.