TSEN15
tRNA splicing endonuclease subunit 15
Summary
This gene encodes a subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from tRNA precursors. Alternative splicing results in multiple transcript variants. There is a pseudogene of this gene on chromosome 17. [provided by RefSeq, Jul 2014]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs73050969 | 1:184,020,763 | C/T | — | benign |
| rs61738765 | 1:184,020,821 | G/A | — | benign |
| rs61738771 | 1:184,020,849 | C/A | — | benign |
| rs1373388521 | 1:184,020,885 | C/T | — | likely benign |
| rs777446348 | 1:184,020,902 | G/A | — | uncertain significance |
| rs1445474819 | 1:184,020,911 | G/C | — | uncertain significance |
| rs1650050859 | 1:184,020,917 | A/G | — | uncertain significance |
| rs776676656 | 1:184,020,920 | C/A | — | uncertain significance |
| rs953562498 | 1:184,020,925 | C/T | — | likely benign |
| rs759083409 | 1:184,020,929 | A/G | — | uncertain significance |
| rs199604629 | 1:184,020,935 | C/A | — | likely benign |
| rs2274432 | 1:184,020,945 | G/A | missense variant | benign |
| rs756147466 | 1:184,020,956 | G/C | — | uncertain significance |
| rs1020949674 | 1:184,020,965 | G/T | — | uncertain significance |
| rs1472696386 | 1:184,020,974 | G/A | — | uncertain significance |
| rs58073693 | 1:184,021,133 | C/T | — | likely benign |
| rs116042970 | 1:184,021,321 | G/A | — | likely benign |
| rs1046934 | 1:184,023,529 | A/C | missense variant | benign |
| rs138058406 | 1:184,023,541 | G/A | — | likely benign |
| rs181137875 | 1:184,023,667 | T/C | — | likely benign |
| rs79391429 | 1:184,023,846 | A/G | — | benign |
| rs730882223 | 1:184,023,870 | T/G | missense variant | pathogenic |
| rs1557877253 | 1:184,023,885 | T/C | — | uncertain significance |
| rs2526465115 | 1:184,023,929 | T/G | — | likely benign |
| rs1046937 | 1:184,023,946 | G/C | — | uncertain significance |
| rs879253780 | 1:184,023,990 | C/T | missense variant | pathogenic |
| rs6664052 | 1:184,024,119 | A/G | — | benign |
| rs114324424 | 1:184,024,278 | G/A | — | likely benign |
| rs1952256 | 1:184,035,116 | A/G | intron variant | — |
| rs41263658 | 1:184,041,257 | G/A | — | likely benign |
| rs184488794 | 1:184,041,317 | G/A | — | uncertain significance |
| rs375946603 | 1:184,041,348 | G/A | — | uncertain significance |
| rs374264447 | 1:184,041,385 | A/G | — | uncertain significance |
| rs879253779 | 1:184,041,392 | A/G | missense variant | pathogenic |
| rs2526527446 | 1:184,041,426 | C/A | — | uncertain significance |
| rs146745937 | 1:184,041,486 | G/A | — | likely benign |
| rs57880810 | 1:184,041,726 | G/A | — | benign |
| rs115409590 | 1:184,041,919 | G/T | — | likely benign |
| rs11549003 | 1:184,042,058 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.