KANSL1L
KAT8 regulatory NSL complex subunit 1 like
Summary
Predicted to enable histone acetyltransferase binding activity. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be part of NSL complex. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746610175 | 2:210,887,713 | G/T | — | uncertain significance |
| rs117674897 | 2:210,887,734 | T/C | — | benign |
| rs151211217 | 2:210,887,737 | G/A | — | uncertain significance |
| rs1190773371 | 2:210,887,787 | T/G | — | uncertain significance |
| rs2093883589 | 2:210,887,861 | C/T | — | uncertain significance |
| rs764940486 | 2:210,889,931 | G/C | — | uncertain significance |
| rs2471443519 | 2:210,892,040 | A/G | — | uncertain significance |
| rs200071643 | 2:210,892,041 | T/G | — | uncertain significance |
| rs201412618 | 2:210,892,066 | A/G | — | uncertain significance |
| rs150714258 | 2:210,893,584 | T/G | — | uncertain significance |
| rs766506680 | 2:210,893,605 | A/G | — | uncertain significance |
| rs755154651 | 2:210,893,620 | A/G | — | uncertain significance |
| rs768167130 | 2:210,893,683 | C/T | — | uncertain significance |
| rs2471462263 | 2:210,894,579 | A/G | — | uncertain significance |
| rs749821746 | 2:210,896,181 | C/T | — | uncertain significance |
| rs775251631 | 2:210,896,250 | A/G | — | uncertain significance |
| rs143376566 | 2:210,896,260 | A/G | — | likely benign |
| rs1431146956 | 2:210,896,270 | A/G | — | uncertain significance |
| rs745507577 | 2:210,908,754 | A/T | — | uncertain significance |
| rs2471554441 | 2:210,908,785 | A/T | — | uncertain significance |
| rs116598794 | 2:210,914,861 | C/G | regulatory region variant | — |
| rs773815030 | 2:210,940,363 | C/T | — | uncertain significance |
| rs575813060 | 2:210,940,376 | G/C | — | uncertain significance |
| rs2041654 | 2:210,953,067 | G/A | coding sequence variant | — |
| rs762505094 | 2:210,968,836 | C/T | — | uncertain significance |
| rs767763798 | 2:210,968,844 | C/T | — | uncertain significance |
| rs745707638 | 2:210,968,920 | C/A | — | uncertain significance |
| rs79865329 | 2:210,968,966 | T/C | — | benign |
| rs200793082 | 2:210,968,969 | C/A | — | likely benign |
| rs115969092 | 2:210,992,363 | A/T | intron variant | — |
| rs958870530 | 2:210,993,762 | G/A | — | uncertain significance |
| rs1286320265 | 2:210,993,855 | C/T | — | uncertain significance |
| rs778583795 | 2:210,993,889 | T/C | — | uncertain significance |
| rs2469082600 | 2:211,018,311 | C/G | — | uncertain significance |
| rs1019938905 | 2:211,018,508 | G/A | — | uncertain significance |
| rs765939208 | 2:211,018,524 | C/T | — | uncertain significance |
| rs2469088521 | 2:211,018,642 | G/A | — | uncertain significance |
| rs148825055 | 2:211,018,702 | G/A | — | likely benign |
| rs2469092322 | 2:211,018,817 | C/G | — | uncertain significance |
| rs769405994 | 2:211,018,882 | G/A | — | uncertain significance |
| rs2095320893 | 2:211,018,943 | T/G | — | uncertain significance |
| rs749378616 | 2:211,018,990 | C/T | — | uncertain significance |
| rs773636479 | 2:211,019,012 | T/G | — | uncertain significance |
| rs1480876320 | 2:211,019,055 | T/A | — | likely benign |
| rs1344190044 | 2:211,019,120 | C/T | — | uncertain significance |
| rs35034344 | 2:211,026,796 | A/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.