TTC7B
tetratricopeptide repeat domain 7B
Summary
Involved in phosphatidylinositol phosphate biosynthetic process and protein localization to plasma membrane. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1452590673 | 14:91,007,798 | C/A | — | uncertain significance |
| rs368249253 | 14:91,007,882 | G/A | — | uncertain significance |
| rs1307560995 | 14:91,007,903 | T/G | — | uncertain significance |
| rs17793829 | 14:91,022,185 | C/T | intron variant | — |
| rs367947343 | 14:91,044,512 | G/A | — | uncertain significance |
| rs752322173 | 14:91,044,518 | C/T | — | uncertain significance |
| rs199934670 | 14:91,044,533 | G/A | — | uncertain significance |
| rs140726085 | 14:91,044,536 | G/T | — | benign |
| rs775739641 | 14:91,044,604 | G/C | — | uncertain significance |
| rs2503499746 | 14:91,059,861 | C/A | — | uncertain significance |
| rs754211574 | 14:91,059,866 | G/A | — | uncertain significance |
| rs138063412 | 14:91,059,965 | C/T | — | uncertain significance |
| rs774719718 | 14:91,077,156 | T/G | — | uncertain significance |
| rs373513556 | 14:91,077,172 | C/T | — | uncertain significance |
| rs2503536169 | 14:91,084,287 | G/T | — | uncertain significance |
| rs370311459 | 14:91,084,351 | C/T | — | uncertain significance |
| rs769715796 | 14:91,084,381 | A/G | — | uncertain significance |
| rs200529596 | 14:91,110,417 | G/C | — | uncertain significance |
| rs564080601 | 14:91,110,426 | C/T | — | uncertain significance |
| rs1462120287 | 14:91,110,429 | T/C | — | uncertain significance |
| rs2503578018 | 14:91,110,542 | G/C | — | uncertain significance |
| rs375472472 | 14:91,113,306 | T/C | — | uncertain significance |
| rs144953526 | 14:91,113,320 | G/C | — | uncertain significance |
| rs149047084 | 14:91,119,219 | C/T | — | uncertain significance |
| rs200578603 | 14:91,121,402 | G/A | — | uncertain significance |
| rs138099673 | 14:91,121,421 | C/T | — | uncertain significance |
| rs745373205 | 14:91,121,439 | T/G | — | uncertain significance |
| rs1325700691 | 14:91,123,535 | T/C | — | uncertain significance |
| rs745988065 | 14:91,124,674 | C/A | — | uncertain significance |
| rs10149267 | 14:91,131,965 | C/T | regulatory region variant | — |
| rs2503635792 | 14:91,142,953 | G/A | — | uncertain significance |
| rs143808424 | 14:91,155,912 | G/A | — | uncertain significance |
| rs1010615036 | 14:91,155,918 | G/A | — | uncertain significance |
| rs147330824 | 14:91,155,947 | C/T | — | uncertain significance |
| rs767851033 | 14:91,155,980 | G/T | — | uncertain significance |
| rs779544238 | 14:91,161,903 | C/T | — | uncertain significance |
| rs561580201 | 14:91,181,098 | G/A | — | — |
| rs767489293 | 14:91,196,448 | C/G | — | uncertain significance |
| rs772642191 | 14:91,196,449 | T/G | — | uncertain significance |
| rs1046828259 | 14:91,247,085 | T/C | — | uncertain significance |
| rs1479552424 | 14:91,247,096 | G/C | — | uncertain significance |
| rs146519690 | 14:91,247,149 | G/A | — | likely benign |
| rs773829725 | 14:91,247,162 | C/T | — | uncertain significance |
| rs200331302 | 14:91,247,241 | G/C | — | uncertain significance |
| rs74085560 | 14:91,252,513 | G/A | — | benign |
| rs771159231 | 14:91,252,558 | C/T | — | uncertain significance |
| rs148256811 | 14:91,252,559 | G/A | — | uncertain significance |
| rs61742122 | 14:91,252,650 | G/A | — | benign |
| rs2503398069 | 14:91,282,611 | A/T | — | uncertain significance |
| rs2503398107 | 14:91,282,629 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.