NFKBIL1
NFKB inhibitor like 1
Summary
This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144672859 | 6:31,516,748 | C/T | upstream gene variant | — |
| rs2523501 | 6:31,517,903 | G/A | — | — |
| rs2516383 | 6:31,519,653 | C/G | — | — |
| rs6916921 | 6:31,520,426 | C/G | — | — |
| rs183526970 | 6:31,520,444 | G/T | upstream gene variant | — |
| rs34492353 | 6:31,520,658 | T/C | — | — |
| rs34268928 | 6:31,521,596 | C/T | intron variant | — |
| rs35597084 | 6:31,523,670 | C/T | intron variant | — |
| rs2857604 | 6:31,525,105 | T/G | intron variant | — |
| rs3093949 | 6:31,525,184 | C/T | intron variant | — |
| rs200454925 | 6:31,525,413 | G/A | — | uncertain significance |
| rs2230365 | 6:31,525,448 | C/T | synonymous variant | benign |
| rs756356865 | 6:31,525,460 | A/G | — | uncertain significance |
| rs373866765 | 6:31,525,522 | C/T | — | uncertain significance |
| rs1261697958 | 6:31,525,536 | G/C | — | uncertain significance |
| rs527461785 | 6:31,525,557 | C/G | — | uncertain significance |
| rs3130062 | 6:31,525,912 | C/T | missense variant | benign |
| rs775101805 | 6:31,525,967 | A/G | — | uncertain significance |
| rs72847261 | 6:31,525,973 | G/A | — | uncertain significance |
| rs139013393 | 6:31,525,988 | G/A | — | uncertain significance |
| rs149963082 | 6:31,525,994 | G/A | — | benign |
| rs200733771 | 6:31,526,056 | C/G | — | likely benign |
| rs1461793520 | 6:31,526,078 | C/G | — | uncertain significance |
| rs184070214 | 6:31,526,080 | G/A | missense variant | — |
| rs373512256 | 6:31,526,129 | G/T | — | uncertain significance |
| rs1208251981 | 6:31,526,365 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.