TTC39A
tetratricopeptide repeat domain 39A
Summary
Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17106487 | 1:51,753,394 | A/G | regulatory region variant | — |
| rs199498888 | 1:51,753,852 | T/C | — | uncertain significance |
| rs2524280578 | 1:51,753,860 | C/T | — | likely benign |
| rs367992416 | 1:51,754,529 | T/C | — | uncertain significance |
| rs372220689 | 1:51,754,551 | C/T | — | uncertain significance |
| rs1553171591 | 1:51,755,680 | G/C | — | uncertain significance |
| rs371947082 | 1:51,755,691 | C/A | — | uncertain significance |
| rs752716688 | 1:51,755,769 | G/C | — | uncertain significance |
| rs1467684561 | 1:51,756,204 | T/A | — | uncertain significance |
| rs144699723 | 1:51,756,228 | C/G | — | uncertain significance |
| rs756251338 | 1:51,756,242 | G/A | — | uncertain significance |
| rs1484889005 | 1:51,756,261 | C/T | — | uncertain significance |
| rs41287288 | 1:51,760,147 | T/C | synonymous variant | — |
| rs776638504 | 1:51,760,156 | A/C | — | uncertain significance |
| rs748363431 | 1:51,767,275 | T/A | — | uncertain significance |
| rs369871888 | 1:51,767,276 | C/T | — | uncertain significance |
| rs1388567653 | 1:51,767,369 | G/C | — | uncertain significance |
| rs199534553 | 1:51,767,396 | G/A | — | uncertain significance |
| rs367944910 | 1:51,768,189 | G/A | — | uncertain significance |
| rs1477925982 | 1:51,768,816 | G/A | — | uncertain significance |
| rs185544961 | 1:51,770,762 | T/C | — | likely benign |
| rs746056817 | 1:51,771,737 | C/A | — | uncertain significance |
| rs75125057 | 1:51,776,342 | G/A | intron variant | — |
| rs375152861 | 1:51,778,521 | C/T | — | uncertain significance |
| rs755415096 | 1:51,787,493 | G/A | — | likely benign |
| rs190460966 | 1:51,796,218 | C/T | — | — |
| rs55681655 | 1:51,801,735 | A/C | downstream gene variant | — |
| rs144982057 | 1:51,807,869 | G/A | regulatory region variant | — |
| rs1310025376 | 1:51,810,684 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.