IRAK2
interleukin 1 receptor associated kinase 2
Summary
IRAK2 encodes the interleukin-1 receptor-associated kinase 2, one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation. IRAK2 is reported to participate in the IL1-induced upregulation of NF-kappaB. [provided by RefSeq, Jul 2008]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141498975 | 3:10,206,204 | C/T | upstream gene variant | — |
| rs146076327 | 3:10,206,637 | C/T | — | likely benign |
| rs1696655413 | 3:10,206,651 | A/G | — | uncertain significance |
| rs201125447 | 3:10,206,655 | A/G | — | uncertain significance |
| rs372088514 | 3:10,219,559 | G/T | — | uncertain significance |
| rs752591902 | 3:10,219,599 | C/T | — | uncertain significance |
| rs150382403 | 3:10,219,600 | G/A | — | uncertain significance |
| rs374194703 | 3:10,219,662 | T/A | — | uncertain significance |
| rs141395070 | 3:10,219,688 | C/T | — | likely benign |
| rs17610943 | 3:10,226,340 | G/A | regulatory region variant | — |
| rs563913827 | 3:10,228,944 | A/T | — | — |
| rs17032518 | 3:10,229,189 | T/C | intron variant | — |
| rs186764169 | 3:10,237,342 | G/A | intron variant | — |
| rs1397867033 | 3:10,242,086 | C/G | — | uncertain significance |
| rs1697340835 | 3:10,242,163 | G/A | — | uncertain significance |
| rs11465886 | 3:10,250,783 | A/G | intron variant | — |
| rs2470235085 | 3:10,251,297 | A/G | — | uncertain significance |
| rs764240479 | 3:10,251,302 | G/A | — | uncertain significance |
| rs141312230 | 3:10,251,350 | G/A | — | likely benign |
| rs2470238358 | 3:10,254,936 | G/A | — | uncertain significance |
| rs56154338 | 3:10,254,968 | C/T | — | likely benign |
| rs35060588 | 3:10,255,002 | C/T | missense variant | — |
| rs201976627 | 3:10,255,042 | G/T | — | uncertain significance |
| rs142327775 | 3:10,255,169 | C/G | — | uncertain significance |
| rs368933968 | 3:10,255,195 | G/A | — | uncertain significance |
| rs201567088 | 3:10,255,225 | T/C | — | uncertain significance |
| rs201789350 | 3:10,258,632 | A/G | — | uncertain significance |
| rs375371662 | 3:10,258,634 | G/T | — | uncertain significance |
| rs780730043 | 3:10,261,371 | C/T | — | uncertain significance |
| rs1457176323 | 3:10,261,377 | C/G | — | uncertain significance |
| rs755590826 | 3:10,261,454 | A/T | — | uncertain significance |
| rs190596152 | 3:10,263,434 | C/T | regulatory region variant | — |
| rs2470248239 | 3:10,264,332 | G/T | — | uncertain significance |
| rs367547215 | 3:10,264,351 | C/T | — | uncertain significance |
| rs1312505692 | 3:10,264,411 | A/G | — | likely benign |
| rs548063415 | 3:10,264,436 | C/T | — | uncertain significance |
| rs944113813 | 3:10,264,447 | T/C | — | uncertain significance |
| rs3844283 | 3:10,264,480 | C/G | — | benign |
| rs752961351 | 3:10,264,490 | G/A | — | uncertain significance |
| rs374087042 | 3:10,268,074 | C/T | — | uncertain significance |
| rs770238130 | 3:10,276,171 | G/C | — | uncertain significance |
| rs1387452834 | 3:10,276,209 | G/A | — | uncertain significance |
| rs1227035262 | 3:10,276,221 | G/T | — | uncertain significance |
| rs200178235 | 3:10,276,284 | G/A | — | likely benign |
| rs2470259766 | 3:10,276,323 | C/T | — | uncertain significance |
| rs74700399 | 3:10,277,804 | G/A | intron variant | — |
| rs760784085 | 3:10,280,462 | C/T | — | uncertain significance |
| rs1288264373 | 3:10,280,505 | C/G | — | uncertain significance |
| rs760388135 | 3:10,280,507 | G/A | — | uncertain significance |
| rs2470264149 | 3:10,280,511 | G/A | — | uncertain significance |
| rs2470264176 | 3:10,280,520 | C/T | — | uncertain significance |
| rs776256963 | 3:10,280,523 | C/T | — | uncertain significance |
| rs145363045 | 3:10,280,552 | G/A | — | uncertain significance |
| rs778357292 | 3:10,280,567 | C/T | — | uncertain significance |
| rs150100488 | 3:10,280,675 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.