TTC38
tetratricopeptide repeat domain 38
Summary
Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74766656 | 22:46,662,497 | A/G | upstream gene variant | — |
| rs961250459 | 22:46,663,961 | G/T | — | uncertain significance |
| rs539833052 | 22:46,664,421 | A/G | — | uncertain significance |
| rs770077600 | 22:46,664,451 | A/G | — | uncertain significance |
| rs374469397 | 22:46,664,483 | A/G | — | uncertain significance |
| rs751400644 | 22:46,668,271 | G/A | — | uncertain significance |
| rs2518738101 | 22:46,668,292 | A/G | — | uncertain significance |
| rs747470323 | 22:46,669,806 | G/A | — | uncertain significance |
| rs377307740 | 22:46,669,837 | C/T | — | uncertain significance |
| rs775281672 | 22:46,669,848 | G/A | — | uncertain significance |
| rs756509394 | 22:46,669,912 | C/T | — | uncertain significance |
| rs369503686 | 22:46,669,938 | G/A | — | uncertain significance |
| rs2518740119 | 22:46,669,950 | G/A | — | uncertain significance |
| rs745824016 | 22:46,671,243 | T/G | — | uncertain significance |
| rs369163736 | 22:46,671,315 | G/A | — | uncertain significance |
| rs138677194 | 22:46,675,727 | G/A | intron variant | — |
| rs370933560 | 22:46,677,505 | A/G | — | uncertain significance |
| rs766399816 | 22:46,677,512 | C/T | — | uncertain significance |
| rs2077535512 | 22:46,677,514 | A/G | — | uncertain significance |
| rs11556946 | 22:46,677,519 | C/G | — | uncertain significance |
| rs368147553 | 22:46,677,527 | C/T | — | uncertain significance |
| rs1263282091 | 22:46,679,871 | A/G | — | uncertain significance |
| rs2518751582 | 22:46,679,885 | G/A | — | uncertain significance |
| rs775427456 | 22:46,679,922 | T/C | — | uncertain significance |
| rs2518752971 | 22:46,681,139 | G/T | — | uncertain significance |
| rs35883013 | 22:46,681,141 | G/A | — | likely benign |
| rs772943844 | 22:46,681,157 | T/G | — | uncertain significance |
| rs2518754682 | 22:46,682,971 | T/C | — | uncertain significance |
| rs562152664 | 22:46,683,036 | C/T | — | uncertain significance |
| rs374547791 | 22:46,684,365 | G/A | — | likely benign |
| rs763753465 | 22:46,684,472 | C/T | — | uncertain significance |
| rs201139315 | 22:46,684,473 | G/A | — | likely benign |
| rs56258934 | 22:46,685,334 | G/A | — | uncertain significance |
| rs779112022 | 22:46,685,358 | A/G | — | uncertain significance |
| rs11705624 | 22:46,685,380 | C/T | synonymous variant | — |
| rs762858496 | 22:46,685,394 | G/A | — | uncertain significance |
| rs372817703 | 22:46,685,396 | G/A | — | uncertain significance |
| rs78692941 | 22:46,685,426 | C/T | — | likely benign |
| rs376502778 | 22:46,685,437 | G/C | — | uncertain significance |
| rs200525894 | 22:46,685,736 | A/G | — | uncertain significance |
| rs566988493 | 22:46,685,762 | A/C | — | uncertain significance |
| rs199616473 | 22:46,685,777 | G/A | — | uncertain significance |
| rs555324724 | 22:46,685,795 | C/T | — | uncertain significance |
| rs73886794 | 22:46,687,268 | G/A | intron variant | — |
| rs2077625838 | 22:46,688,722 | A/T | — | uncertain significance |
| rs200604599 | 22:46,688,749 | C/T | — | uncertain significance |
| rs57866552 | 22:46,689,229 | C/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.