AADAC
arylacetamide deacetylase
Summary
Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransferase, which catalyzes one of the initial biotransformation pathways for arylamine and heterocyclic amine carcinogens [provided by RefSeq, Jul 2008]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs552581419 | 3:151,531,965 | G/A | — | likely benign |
| rs550415872 | 3:151,531,994 | T/C | — | uncertain significance |
| rs763301411 | 3:151,532,012 | C/T | — | uncertain significance |
| rs568566549 | 3:151,532,024 | A/T | — | uncertain significance |
| rs771524086 | 3:151,532,065 | C/T | — | uncertain significance |
| rs1409806369 | 3:151,532,082 | A/C | — | uncertain significance |
| rs2472967053 | 3:151,535,206 | T/A | — | uncertain significance |
| rs1344987591 | 3:151,535,226 | G/A | — | uncertain significance |
| rs143156740 | 3:151,535,244 | G/A | — | uncertain significance |
| rs2472967267 | 3:151,535,305 | A/G | — | uncertain significance |
| rs746954617 | 3:151,538,171 | C/G | — | uncertain significance |
| rs756073579 | 3:151,542,525 | G/A | — | uncertain significance |
| rs369720545 | 3:151,542,575 | T/G | — | uncertain significance |
| rs748717673 | 3:151,545,380 | A/T | — | uncertain significance |
| rs1228282097 | 3:151,545,381 | T/A | — | uncertain significance |
| rs151039277 | 3:151,545,447 | A/C | — | uncertain significance |
| rs1457066577 | 3:151,545,469 | A/T | — | uncertain significance |
| rs766695796 | 3:151,545,716 | C/A | — | uncertain significance |
| rs772674234 | 3:151,545,748 | C/T | — | uncertain significance |
| rs755736454 | 3:151,545,836 | C/T | — | uncertain significance |
| rs146149654 | 3:151,545,847 | G/A | — | uncertain significance |
| rs187652875 | 3:151,545,886 | T/C | — | uncertain significance |
| rs1576647382 | 3:151,545,930 | G/T | — | uncertain significance |
| rs766697843 | 3:151,545,932 | A/G | — | uncertain significance |
| rs1576647402 | 3:151,545,953 | A/C | — | uncertain significance |
| rs61733692 | 3:151,545,958 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.