TCP11
t-complex 11
Summary
Involved in germ cell development. Located in acrosomal vesicle and sperm flagellum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1369129582 | 6:35,086,276 | G/C | — | uncertain significance |
| rs777371930 | 6:35,087,067 | G/A | — | uncertain significance |
| rs142229547 | 6:35,087,068 | C/T | — | uncertain significance |
| rs2234046 | 6:35,088,018 | C/T | — | uncertain significance |
| rs376470025 | 6:35,088,285 | G/A | — | uncertain significance |
| rs776312603 | 6:35,088,423 | C/T | — | uncertain significance |
| rs1349735266 | 6:35,088,730 | T/G | — | uncertain significance |
| rs371137302 | 6:35,088,811 | T/G | — | uncertain significance |
| rs2533337758 | 6:35,088,820 | C/T | — | uncertain significance |
| rs199753305 | 6:35,089,976 | T/C | — | uncertain significance |
| rs372296449 | 6:35,089,978 | T/C | — | uncertain significance |
| rs375000730 | 6:35,090,015 | C/A | — | uncertain significance |
| rs761880060 | 6:35,090,033 | G/C | — | uncertain significance |
| rs755441742 | 6:35,090,065 | A/G | — | uncertain significance |
| rs1779362891 | 6:35,090,072 | T/C | — | uncertain significance |
| rs2395609 | 6:35,094,150 | G/C | intron variant | — |
| rs147549679 | 6:35,096,933 | A/G | — | uncertain significance |
| rs1475863816 | 6:35,096,951 | C/T | — | uncertain significance |
| rs34523546 | 6:35,099,094 | C/T | upstream gene variant | — |
| rs754716204 | 6:35,103,975 | T/A | — | uncertain significance |
| rs745455902 | 6:35,108,530 | G/T | — | uncertain significance |
| rs779675502 | 6:35,108,533 | G/T | — | uncertain significance |
| rs755782847 | 6:35,108,566 | G/A | — | uncertain significance |
| rs543124451 | 6:35,108,595 | C/T | — | uncertain significance |
| rs745687408 | 6:35,109,002 | G/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.