TTC28
tetratricopeptide repeat domain 28
Summary
Enables kinase binding activity. Involved in regulation of mitotic cell cycle. Located in midbody. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants204 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs78554043 | 22:28,374,943 | G/C | 3 prime UTR variant | — |
| rs1032307071 | 22:28,378,289 | C/T | — | likely benign |
| rs199899926 | 22:28,378,294 | G/A | — | uncertain significance |
| rs548924832 | 22:28,378,312 | G/A | — | uncertain significance |
| rs887416829 | 22:28,378,336 | G/A | — | uncertain significance |
| rs56085644 | 22:28,378,351 | C/T | — | conflicting classifications of pathogenicity |
| rs41278845 | 22:28,378,384 | G/C | — | benign |
| rs201938772 | 22:28,378,458 | T/C | — | likely benign |
| rs5762430 | 22:28,378,472 | A/T | missense variant | — |
| rs573932994 | 22:28,378,520 | G/A | — | uncertain significance |
| rs960596602 | 22:28,378,524 | G/C | — | uncertain significance |
| rs775874303 | 22:28,378,624 | T/G | — | uncertain significance |
| rs1460172382 | 22:28,378,657 | C/G | — | uncertain significance |
| rs2517640095 | 22:28,378,661 | C/T | — | uncertain significance |
| rs1601475038 | 22:28,378,785 | G/A | — | likely benign |
| rs370917225 | 22:28,378,839 | G/A | — | likely benign |
| rs923669430 | 22:28,378,850 | G/A | — | uncertain significance |
| rs758631680 | 22:28,378,952 | G/T | — | uncertain significance |
| rs1937075147 | 22:28,378,988 | T/C | — | uncertain significance |
| rs189781469 | 22:28,379,016 | C/T | — | likely benign |
| rs5762431 | 22:28,379,058 | C/T | — | benign |
| rs780074002 | 22:28,379,059 | G/A | — | likely benign |
| rs538752652 | 22:28,379,066 | C/T | — | likely benign |
| rs1937079206 | 22:28,379,069 | C/T | — | uncertain significance |
| rs747169297 | 22:28,379,096 | C/A | — | uncertain significance |
| rs143432636 | 22:28,379,120 | G/A | — | conflicting classifications of pathogenicity |
| rs764330777 | 22:28,379,128 | G/T | — | uncertain significance |
| rs909480025 | 22:28,379,216 | C/T | — | uncertain significance |
| rs1347230179 | 22:28,379,245 | T/C | — | uncertain significance |
| rs77293143 | 22:28,379,262 | T/A | — | benign |
| rs769824236 | 22:28,379,395 | G/T | — | uncertain significance |
| rs2517644856 | 22:28,379,481 | C/G | — | likely benign |
| rs746058646 | 22:28,379,581 | C/G | — | uncertain significance |
| rs986600100 | 22:28,379,597 | G/A | — | uncertain significance |
| rs760382704 | 22:28,379,703 | G/T | — | uncertain significance |
| rs376130030 | 22:28,379,714 | C/T | — | uncertain significance |
| rs61739455 | 22:28,379,715 | G/A | — | benign |
| rs376514291 | 22:28,381,279 | G/A | — | uncertain significance |
| rs1485205249 | 22:28,381,281 | C/T | — | uncertain significance |
| rs2517652142 | 22:28,381,308 | A/C | — | uncertain significance |
| rs574557756 | 22:28,381,326 | A/G | — | uncertain significance |
| rs756460879 | 22:28,385,885 | G/A | — | likely benign |
| rs1194901069 | 22:28,385,914 | C/T | — | uncertain significance |
| rs1016516249 | 22:28,385,968 | C/A | — | uncertain significance |
| rs41281595 | 22:28,388,576 | C/T | — | uncertain significance |
| rs747516056 | 22:28,388,597 | G/C | — | uncertain significance |
| rs191320855 | 22:28,389,314 | G/A | — | likely benign |
| rs764243881 | 22:28,389,322 | G/A | — | uncertain significance |
| rs867127532 | 22:28,389,326 | C/T | — | uncertain significance |
| rs575074859 | 22:28,389,365 | T/C | — | likely benign |
| rs200365104 | 22:28,389,379 | C/T | — | likely benign |
| rs369701523 | 22:28,389,422 | C/T | — | uncertain significance |
| rs1937486999 | 22:28,389,433 | T/C | — | uncertain significance |
| rs748910267 | 22:28,389,469 | C/T | — | uncertain significance |
| rs927732535 | 22:28,392,127 | T/C | — | uncertain significance |
| rs980646124 | 22:28,392,139 | C/T | — | uncertain significance |
| rs180717177 | 22:28,392,157 | C/T | — | uncertain significance |
| rs572257896 | 22:28,392,162 | C/T | — | likely benign |
| rs1336312569 | 22:28,392,179 | C/G | — | uncertain significance |
| rs554709872 | 22:28,392,729 | G/A | — | — |
| rs1392554521 | 22:28,394,542 | G/A | — | uncertain significance |
| rs758676588 | 22:28,394,612 | C/T | — | uncertain significance |
| rs187345071 | 22:28,394,685 | G/A | — | benign |
| rs758115230 | 22:28,394,699 | C/T | — | uncertain significance |
| rs2517697826 | 22:28,394,831 | G/A | — | uncertain significance |
| rs1207483285 | 22:28,394,896 | C/T | — | uncertain significance |
| rs371431041 | 22:28,394,928 | G/A | — | likely benign |
| rs961995309 | 22:28,395,065 | C/T | — | uncertain significance |
| rs369845727 | 22:28,395,101 | C/T | — | uncertain significance |
| rs866979937 | 22:28,395,189 | G/C | — | uncertain significance |
| rs1239732922 | 22:28,395,199 | G/A | — | uncertain significance |
| rs1040804323 | 22:28,395,202 | A/G | — | uncertain significance |
| rs182798052 | 22:28,395,218 | A/C | — | uncertain significance |
| rs748850926 | 22:28,395,238 | C/T | — | uncertain significance |
| rs929418597 | 22:28,395,239 | G/A | — | uncertain significance |
| rs932835381 | 22:28,395,252 | G/A | — | likely benign |
| rs564603781 | 22:28,397,419 | G/A | — | likely benign |
| rs1937687404 | 22:28,397,441 | C/G | — | uncertain significance |
| rs548381923 | 22:28,397,481 | C/A | — | uncertain significance |
| rs760175692 | 22:28,397,504 | C/T | — | uncertain significance |
| rs61744141 | 22:28,397,505 | G/A | — | conflicting classifications of pathogenicity |
| rs753773499 | 22:28,397,510 | C/T | — | uncertain significance |
| rs1216824328 | 22:28,397,518 | G/A | — | likely benign |
| rs374539679 | 22:28,397,523 | C/T | — | uncertain significance |
| rs1402461034 | 22:28,410,273 | C/T | — | uncertain significance |
| rs763076899 | 22:28,410,282 | G/A | — | uncertain significance |
| rs61739502 | 22:28,410,313 | G/C | — | benign |
| rs763825504 | 22:28,410,325 | C/T | — | uncertain significance |
| rs200471285 | 22:28,410,336 | G/A | — | uncertain significance |
| rs755114255 | 22:28,410,363 | G/A | — | uncertain significance |
| rs1355484587 | 22:28,426,230 | T/G | — | uncertain significance |
| rs201500299 | 22:28,426,233 | G/A | — | uncertain significance |
| rs771335791 | 22:28,426,236 | G/A | — | uncertain significance |
| rs961236168 | 22:28,426,245 | G/A | — | uncertain significance |
| rs941560744 | 22:28,426,248 | G/C | — | uncertain significance |
| rs745548425 | 22:28,426,270 | C/T | — | likely benign |
| rs1266189120 | 22:28,426,293 | C/T | — | uncertain significance |
| rs34564977 | 22:28,433,235 | C/T | — | — |
| rs143459581 | 22:28,464,850 | C/T | intron variant | — |
| rs758943310 | 22:28,490,101 | C/T | — | uncertain significance |
Showing 100 of 204 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.