KANSL3
KAT8 regulatory NSL complex subunit 3
Summary
Involved in regulation of mitochondrial transcription. Located in mitochondrion and nucleoplasm. Part of NSL complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11676886 | 2:97,249,011 | A/G | intergenic variant | — |
| rs1209781034 | 2:97,261,367 | C/T | — | uncertain significance |
| rs748490637 | 2:97,267,426 | G/A | — | uncertain significance |
| rs2468190500 | 2:97,267,457 | T/A | — | uncertain significance |
| rs767434248 | 2:97,267,961 | T/C | — | uncertain significance |
| rs767197678 | 2:97,268,041 | C/T | — | uncertain significance |
| rs780767760 | 2:97,268,533 | G/A | — | uncertain significance |
| rs116798525 | 2:97,270,008 | A/C | — | likely benign |
| rs2468347681 | 2:97,270,013 | G/A | — | uncertain significance |
| rs533700327 | 2:97,270,022 | C/T | — | uncertain significance |
| rs2468356676 | 2:97,270,106 | G/A | — | uncertain significance |
| rs2468390571 | 2:97,270,552 | C/A | — | uncertain significance |
| rs2468428849 | 2:97,271,066 | C/T | — | uncertain significance |
| rs1333043887 | 2:97,271,081 | G/C | — | uncertain significance |
| rs370312220 | 2:97,271,140 | C/A | — | uncertain significance |
| rs200065186 | 2:97,271,152 | T/G | — | uncertain significance |
| rs756916398 | 2:97,271,179 | T/C | — | uncertain significance |
| rs1573347802 | 2:97,271,208 | C/A | — | uncertain significance |
| rs1266509595 | 2:97,271,210 | C/T | — | uncertain significance |
| rs145222575 | 2:97,274,268 | A/G | — | uncertain significance |
| rs369470185 | 2:97,274,358 | G/A | — | uncertain significance |
| rs536572106 | 2:97,274,636 | C/G | — | uncertain significance |
| rs754040533 | 2:97,274,690 | G/A | — | uncertain significance |
| rs922744856 | 2:97,274,702 | G/A | — | uncertain significance |
| rs776152330 | 2:97,274,765 | G/A | — | uncertain significance |
| rs2068443939 | 2:97,274,776 | C/A | — | uncertain significance |
| rs2468688528 | 2:97,274,791 | A/G | — | uncertain significance |
| rs2068446852 | 2:97,274,799 | A/C | — | uncertain significance |
| rs371529777 | 2:97,276,484 | C/A | — | uncertain significance |
| rs748810614 | 2:97,276,544 | G/T | — | uncertain significance |
| rs2468826758 | 2:97,276,587 | G/C | — | uncertain significance |
| rs372683631 | 2:97,278,052 | A/C | — | uncertain significance |
| rs763749843 | 2:97,278,053 | A/G | — | uncertain significance |
| rs2468922367 | 2:97,278,069 | T/G | — | uncertain significance |
| rs370777860 | 2:97,278,227 | A/G | — | uncertain significance |
| rs1413235727 | 2:97,278,620 | T/A | — | uncertain significance |
| rs201372384 | 2:97,279,225 | T/C | — | uncertain significance |
| rs2469005896 | 2:97,279,307 | C/G | — | uncertain significance |
| rs2468089591 | 2:97,285,464 | T/A | — | uncertain significance |
| rs2070890346 | 2:97,285,473 | T/C | — | uncertain significance |
| rs370590181 | 2:97,285,486 | T/C | — | uncertain significance |
| rs374477720 | 2:97,297,173 | T/C | — | likely benign |
| rs748315929 | 2:97,297,184 | G/A | — | uncertain significance |
| rs760552557 | 2:97,297,209 | C/A | — | uncertain significance |
| rs2468636265 | 2:97,302,704 | T/C | — | uncertain significance |
| rs2468638308 | 2:97,302,730 | T/C | — | uncertain significance |
| rs1159145743 | 2:97,302,860 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.