TDRD12
tudor domain containing 12
Summary
Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and RNA helicase activity. Predicted to be involved in several processes, including germ-line stem cell division; male meiotic nuclear division; and regulatory ncRNA-mediated gene silencing. Predicted to be part of PET complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs508455 | 19:33,216,592 | G/A | intron variant | — |
| rs1447586209 | 19:33,222,664 | A/G | — | uncertain significance |
| rs1969063673 | 19:33,222,688 | C/G | — | uncertain significance |
| rs937793522 | 19:33,222,697 | G/A | — | uncertain significance |
| rs1196825700 | 19:33,229,766 | G/T | — | uncertain significance |
| rs1389732114 | 19:33,229,811 | T/C | — | uncertain significance |
| rs767866241 | 19:33,229,823 | C/A | — | uncertain significance |
| rs1305879579 | 19:33,229,831 | G/A | — | uncertain significance |
| rs201742920 | 19:33,229,861 | G/A | — | uncertain significance |
| rs1220731349 | 19:33,229,865 | A/C | — | uncertain significance |
| rs111959637 | 19:33,231,028 | C/A | — | — |
| rs191078032 | 19:33,233,697 | G/A | — | uncertain significance |
| rs1258798258 | 19:33,233,700 | G/T | — | uncertain significance |
| rs775908730 | 19:33,233,749 | A/G | — | uncertain significance |
| rs200157515 | 19:33,239,402 | A/G | — | likely benign |
| rs955845538 | 19:33,239,407 | G/T | — | uncertain significance |
| rs1370192431 | 19:33,239,416 | T/C | — | uncertain significance |
| rs1969724820 | 19:33,239,419 | T/C | — | uncertain significance |
| rs754053658 | 19:33,246,908 | A/G | — | uncertain significance |
| rs553356119 | 19:33,246,949 | C/T | — | uncertain significance |
| rs1019504812 | 19:33,246,959 | A/C | — | uncertain significance |
| rs919758554 | 19:33,247,067 | A/G | — | uncertain significance |
| rs2513293584 | 19:33,247,944 | A/G | — | uncertain significance |
| rs1329890348 | 19:33,247,974 | C/T | — | uncertain significance |
| rs1442618813 | 19:33,248,024 | G/A | — | uncertain significance |
| rs781292950 | 19:33,263,696 | T/A | — | conflicting classifications of pathogenicity |
| rs1176835993 | 19:33,263,757 | G/T | — | likely pathogenic |
| rs2513339653 | 19:33,264,384 | G/A | — | likely pathogenic |
| rs2513339855 | 19:33,264,403 | A/G | — | uncertain significance |
| rs58026555 | 19:33,265,013 | A/G | intron variant | — |
| rs182893165 | 19:33,274,051 | G/A | intron variant | — |
| rs2513399397 | 19:33,281,467 | G/C | — | uncertain significance |
| rs768268292 | 19:33,281,471 | G/T | — | uncertain significance |
| rs34982176 | 19:33,285,684 | G/A | — | benign |
| rs140337503 | 19:33,291,210 | C/T | — | likely benign |
| rs541196125 | 19:33,293,908 | C/T | — | likely benign |
| rs745891404 | 19:33,293,915 | C/T | — | likely pathogenic |
| rs1262515590 | 19:33,293,928 | G/A | — | conflicting classifications of pathogenicity |
Gene information from NCBI Gene. Variant classifications from ClinVar.