TRAFD1
TRAF-type zinc finger domain containing 1
Summary
The innate immune system confers host defense against viral and microbial infection, and TRAFD1 is a negative feedback regulator that controls excessive immune responses (Sanada et al., 2008 [PubMed 18849341]).[supplied by OMIM, Dec 2009]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2499688811 | 12:112,568,355 | C/A | — | uncertain significance |
| rs368919929 | 12:112,572,606 | A/G | — | likely benign |
| rs768638859 | 12:112,572,652 | C/G | — | uncertain significance |
| rs147782156 | 12:112,572,660 | G/A | — | uncertain significance |
| rs569633774 | 12:112,572,830 | G/T | — | uncertain significance |
| rs12231737 | 12:112,574,616 | C/T | intron variant | — |
| rs535526948 | 12:112,576,832 | T/A | — | — |
| rs1593868089 | 12:112,578,707 | T/G | — | uncertain significance |
| rs2499698282 | 12:112,578,779 | C/G | — | uncertain significance |
| rs780551409 | 12:112,578,782 | G/C | — | uncertain significance |
| rs149081968 | 12:112,578,799 | G/C | — | likely benign |
| rs201656998 | 12:112,578,820 | G/C | — | uncertain significance |
| rs769372382 | 12:112,578,890 | C/T | — | uncertain significance |
| rs61740854 | 12:112,579,945 | G/A | — | benign |
| rs560633197 | 12:112,580,049 | G/A | — | uncertain significance |
| rs114577048 | 12:112,580,072 | G/A | — | uncertain significance |
| rs2499706861 | 12:112,586,001 | G/C | — | uncertain significance |
| rs147745928 | 12:112,589,629 | A/G | — | uncertain significance |
| rs145065325 | 12:112,589,679 | A/G | — | uncertain significance |
| rs749334114 | 12:112,589,685 | C/T | — | uncertain significance |
| rs190153144 | 12:112,589,686 | C/G | — | uncertain significance |
| rs1236845359 | 12:112,589,731 | C/T | — | uncertain significance |
| rs753181748 | 12:112,589,745 | C/G | — | uncertain significance |
| rs200338185 | 12:112,589,815 | G/A | — | likely benign |
| rs756571103 | 12:112,589,850 | G/A | — | uncertain significance |
| rs371539929 | 12:112,589,905 | C/T | — | uncertain significance |
| rs2499711325 | 12:112,590,247 | G/A | — | uncertain significance |
| rs150138091 | 12:112,590,254 | A/C | — | uncertain significance |
| rs771826384 | 12:112,590,259 | C/T | — | uncertain significance |
| rs2499711405 | 12:112,590,271 | G/T | — | uncertain significance |
| rs2499711765 | 12:112,590,569 | G/C | — | uncertain significance |
| rs182634285 | 12:112,591,854 | T/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.