NAT16
N-acetyltransferase 16 (putative)
Summary
Predicted to enable acyltransferase activity, transferring groups other than amino-acyl groups. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201313983 | 7:100,815,373 | T/C | — | uncertain significance |
| rs756647344 | 7:100,815,466 | A/C | — | uncertain significance |
| rs1256631359 | 7:100,815,613 | A/G | — | uncertain significance |
| rs1253705388 | 7:100,815,659 | G/A | — | uncertain significance |
| rs1797345427 | 7:100,815,668 | C/A | — | uncertain significance |
| rs550665110 | 7:100,815,670 | C/A | — | uncertain significance |
| rs1037529011 | 7:100,815,697 | A/T | — | uncertain significance |
| rs759287497 | 7:100,815,760 | A/C | — | uncertain significance |
| rs762206776 | 7:100,815,765 | G/C | — | likely benign |
| rs1399359434 | 7:100,815,862 | C/T | — | uncertain significance |
| rs879584444 | 7:100,815,863 | G/C | — | uncertain significance |
| rs766793827 | 7:100,815,899 | G/C | — | uncertain significance |
| rs740104 | 7:100,816,347 | C/T | — | — |
| rs1254747811 | 7:100,816,593 | C/T | — | uncertain significance |
| rs569010209 | 7:100,816,669 | T/C | — | uncertain significance |
| rs1407555880 | 7:100,816,672 | T/C | — | uncertain significance |
| rs762778679 | 7:100,816,726 | C/T | — | uncertain significance |
| rs746429184 | 7:100,816,737 | A/G | — | uncertain significance |
| rs747518733 | 7:100,816,747 | C/G | — | uncertain significance |
| rs375132035 | 7:100,816,761 | G/T | — | uncertain significance |
| rs770154793 | 7:100,816,768 | C/T | — | uncertain significance |
| rs141085888 | 7:100,817,818 | G/T | — | uncertain significance |
| rs201666132 | 7:100,817,874 | C/A | — | uncertain significance |
| rs750463591 | 7:100,817,878 | C/G | — | uncertain significance |
| rs34985488 | 7:100,817,901 | A/C | missense variant | — |
| rs868016095 | 7:100,817,958 | G/A | — | uncertain significance |
| rs200814753 | 7:100,817,970 | G/C | — | uncertain significance |
| rs867086471 | 7:100,818,015 | G/C | — | uncertain significance |
| rs555118087 | 7:100,818,028 | T/C | — | likely benign |
| rs143939241 | 7:100,818,039 | G/A | — | uncertain significance |
| rs773603616 | 7:100,818,042 | T/C | — | uncertain significance |
| rs767752008 | 7:100,818,075 | G/T | — | uncertain significance |
| rs61731322 | 7:100,823,629 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.