AKNA
AT-hook transcription factor
Summary
Predicted to enable DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in centrosome; cytosol; and nuclear lumen. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants123 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1248345034 | 9:117,099,363 | G/A | — | uncertain significance |
| rs776409662 | 9:117,099,371 | C/T | — | uncertain significance |
| rs772806799 | 9:117,099,375 | G/T | — | uncertain significance |
| rs144685609 | 9:117,099,389 | G/A | — | uncertain significance |
| rs750525549 | 9:117,099,401 | T/C | — | uncertain significance |
| rs369108374 | 9:117,099,417 | G/A | — | uncertain significance |
| rs376756585 | 9:117,099,429 | C/T | — | uncertain significance |
| rs1410563869 | 9:117,099,444 | G/A | — | uncertain significance |
| rs375161600 | 9:117,099,483 | C/T | — | uncertain significance |
| rs774022950 | 9:117,099,497 | T/A | — | uncertain significance |
| rs542469768 | 9:117,099,518 | G/T | — | uncertain significance |
| rs768927736 | 9:117,103,867 | G/A | — | uncertain significance |
| rs181195161 | 9:117,103,930 | G/A | — | uncertain significance |
| rs140345797 | 9:117,103,987 | G/A | — | uncertain significance |
| rs764786775 | 9:117,104,306 | G/C | — | uncertain significance |
| rs753965064 | 9:117,104,330 | C/T | — | uncertain significance |
| rs961038334 | 9:117,104,340 | C/T | — | uncertain significance |
| rs770214671 | 9:117,108,197 | C/G | — | uncertain significance |
| rs199693279 | 9:117,108,220 | T/C | — | uncertain significance |
| rs757706175 | 9:117,108,996 | C/T | — | uncertain significance |
| rs893747712 | 9:117,110,010 | T/C | — | uncertain significance |
| rs1265211690 | 9:117,110,025 | G/A | — | uncertain significance |
| rs747494693 | 9:117,110,029 | C/T | — | uncertain significance |
| rs768894874 | 9:117,110,034 | G/T | — | uncertain significance |
| rs769845922 | 9:117,110,047 | G/A | — | uncertain significance |
| rs573540327 | 9:117,110,050 | C/T | — | uncertain significance |
| rs573168301 | 9:117,110,058 | C/T | — | uncertain significance |
| rs62640059 | 9:117,110,092 | T/C | — | likely benign |
| rs766904268 | 9:117,110,133 | C/T | — | uncertain significance |
| rs575149664 | 9:117,110,139 | C/T | — | uncertain significance |
| rs143050232 | 9:117,110,140 | G/A | — | uncertain significance |
| rs145218351 | 9:117,110,160 | T/C | — | benign |
| rs201422989 | 9:117,113,154 | G/A | — | uncertain significance |
| rs775868517 | 9:117,113,187 | C/T | — | uncertain significance |
| rs750708829 | 9:117,113,202 | G/A | — | uncertain significance |
| rs726891 | 9:117,113,207 | G/A | — | benign |
| rs146410512 | 9:117,118,217 | C/T | — | uncertain significance |
| rs61757559 | 9:117,118,245 | T/C | — | benign |
| rs1831478778 | 9:117,118,315 | T/C | — | uncertain significance |
| rs758074889 | 9:117,118,370 | C/T | — | uncertain significance |
| rs61757558 | 9:117,118,379 | C/T | — | benign |
| rs150349533 | 9:117,119,165 | C/T | — | uncertain significance |
| rs549404488 | 9:117,119,236 | G/A | — | uncertain significance |
| rs200882090 | 9:117,119,242 | C/A | — | uncertain significance |
| rs767673471 | 9:117,120,218 | C/T | — | uncertain significance |
| rs2490907653 | 9:117,120,238 | T/C | — | uncertain significance |
| rs201336367 | 9:117,120,248 | G/A | — | uncertain significance |
| rs754028722 | 9:117,120,290 | G/C | — | uncertain significance |
| rs41312192 | 9:117,120,332 | C/T | — | likely benign |
| rs758290157 | 9:117,120,365 | C/T | — | uncertain significance |
| rs369198137 | 9:117,120,383 | C/T | — | likely benign |
| rs374900536 | 9:117,120,410 | C/G | — | uncertain significance |
| rs1831642834 | 9:117,120,413 | G/A | — | uncertain significance |
| rs1564631978 | 9:117,120,429 | C/T | — | uncertain significance |
| rs2490945443 | 9:117,121,883 | G/A | — | uncertain significance |
| rs369809519 | 9:117,121,908 | C/T | — | uncertain significance |
| rs1424513916 | 9:117,122,029 | C/A | — | uncertain significance |
| rs889110027 | 9:117,122,031 | C/T | — | uncertain significance |
| rs753245670 | 9:117,122,060 | T/C | — | uncertain significance |
| rs750129324 | 9:117,122,179 | T/C | — | uncertain significance |
| rs1241715659 | 9:117,122,221 | T/A | — | uncertain significance |
| rs201036834 | 9:117,122,230 | C/T | — | uncertain significance |
| rs2490957127 | 9:117,122,240 | G/A | — | uncertain significance |
| rs143025426 | 9:117,122,311 | C/A | — | uncertain significance |
| rs10817595 | 9:117,123,750 | C/T | — | — |
| rs45550039 | 9:117,124,045 | A/G | — | likely benign |
| rs1394611046 | 9:117,124,077 | G/A | — | likely benign |
| rs767572273 | 9:117,124,115 | C/T | — | uncertain significance |
| rs534516846 | 9:117,124,125 | C/G | — | uncertain significance |
| rs201526872 | 9:117,124,154 | G/C | — | uncertain significance |
| rs1831995499 | 9:117,124,156 | C/T | — | uncertain significance |
| rs142298734 | 9:117,124,168 | C/T | — | uncertain significance |
| rs200662629 | 9:117,124,169 | G/A | — | uncertain significance |
| rs558018170 | 9:117,124,723 | C/T | — | uncertain significance |
| rs138805714 | 9:117,124,803 | C/T | — | likely benign |
| rs543391673 | 9:117,126,878 | T/G | — | uncertain significance |
| rs368140660 | 9:117,129,908 | G/A | — | uncertain significance |
| rs62640865 | 9:117,129,921 | G/C | — | benign |
| rs146163104 | 9:117,129,940 | C/G | — | benign |
| rs201466935 | 9:117,129,941 | G/A | — | uncertain significance |
| rs758602723 | 9:117,129,949 | G/T | — | uncertain significance |
| rs2491084934 | 9:117,129,965 | G/A | — | uncertain significance |
| rs141152498 | 9:117,130,727 | G/A | — | likely benign |
| rs780905946 | 9:117,130,739 | G/C | — | uncertain significance |
| rs765817954 | 9:117,130,757 | G/A | — | uncertain significance |
| rs1588997765 | 9:117,130,758 | G/A | — | uncertain significance |
| rs60819454 | 9:117,130,776 | G/A | — | benign |
| rs2131983792 | 9:117,130,788 | T/C | — | uncertain significance |
| rs778221993 | 9:117,130,829 | G/A | — | likely benign |
| rs368417179 | 9:117,130,842 | G/A | — | uncertain significance |
| rs7032795 | 9:117,134,945 | T/C | regulatory region variant | — |
| rs4979371 | 9:117,138,278 | C/T | intron variant | — |
| rs747534212 | 9:117,138,783 | G/A | — | uncertain significance |
| rs147861969 | 9:117,138,802 | C/T | — | uncertain significance |
| rs781152372 | 9:117,138,935 | G/T | — | uncertain significance |
| rs372829482 | 9:117,138,937 | G/A | — | uncertain significance |
| rs552700642 | 9:117,139,035 | C/T | — | uncertain significance |
| rs140509220 | 9:117,139,053 | T/C | — | uncertain significance |
| rs200338881 | 9:117,139,062 | G/A | — | uncertain significance |
| rs368308567 | 9:117,139,072 | C/T | — | uncertain significance |
Showing 100 of 123 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.