TRIM38
tripartite motif containing 38
Summary
This gene encodes a member of the tripartite motif (TRIM) family. The encoded protein contains a RING-type zinc finger, B box-type zinc finger and SPRY domain. The function of this protein has not been identified. A pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Jul 2012]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs569918634 | 6:25,965,092 | T/G | — | — |
| rs111268094 | 6:25,965,260 | C/G | intron variant | — |
| rs373694907 | 6:25,966,821 | C/T | — | uncertain significance |
| rs2481387923 | 6:25,966,861 | C/G | — | uncertain significance |
| rs140538175 | 6:25,966,952 | A/G | — | uncertain significance |
| rs761564484 | 6:25,967,066 | G/A | — | uncertain significance |
| rs201589214 | 6:25,967,127 | C/T | — | uncertain significance |
| rs538233068 | 6:25,969,602 | G/T | — | uncertain significance |
| rs182712233 | 6:25,971,350 | C/T | regulatory region variant | — |
| rs750792570 | 6:25,972,127 | C/T | — | uncertain significance |
| rs1465146420 | 6:25,972,181 | C/A | — | uncertain significance |
| rs370611506 | 6:25,972,191 | T/C | — | uncertain significance |
| rs141368509 | 6:25,972,261 | T/A | — | uncertain significance |
| rs200853447 | 6:25,972,296 | A/G | — | uncertain significance |
| rs753646980 | 6:25,973,403 | G/A | — | uncertain significance |
| rs13203673 | 6:25,979,122 | T/C | downstream gene variant | — |
| rs780565429 | 6:25,983,414 | T/A | — | uncertain significance |
| rs146076775 | 6:25,983,427 | G/A | — | uncertain significance |
| rs200555657 | 6:25,983,463 | C/T | — | uncertain significance |
| rs1249488930 | 6:25,983,572 | A/G | — | uncertain significance |
| rs1416672156 | 6:25,983,584 | G/T | — | uncertain significance |
| rs769693795 | 6:25,983,604 | G/A | — | uncertain significance |
| rs766598574 | 6:25,983,713 | C/T | — | uncertain significance |
| rs2481420628 | 6:25,983,767 | A/G | — | uncertain significance |
| rs17528178 | 6:25,983,777 | C/G | synonymous variant | — |
| rs1039205016 | 6:25,983,833 | A/G | — | uncertain significance |
| rs779537642 | 6:25,983,857 | G/A | — | uncertain significance |
| rs777725261 | 6:25,983,904 | C/G | — | uncertain significance |
| rs183879 | 6:25,987,441 | G/T | — | — |
| rs12216125 | 6:25,997,458 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.