AFMID
arylformamidase
Summary
Predicted to enable arylformamidase activity. Predicted to be involved in L-tryptophan catabolic process to kynurenine. Predicted to be located in cytosol and nucleus. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2075820750 | 17:76,183,455 | A/G | — | uncertain significance |
| rs2510904319 | 17:76,187,085 | T/C | — | uncertain significance |
| rs138405849 | 17:76,187,091 | G/A | — | uncertain significance |
| rs77585764 | 17:76,187,108 | G/C | missense variant | — |
| rs72897835 | 17:76,198,530 | T/G | intron variant | — |
| rs769495118 | 17:76,198,676 | C/T | — | uncertain significance |
| rs143224831 | 17:76,198,828 | G/A | — | uncertain significance |
| rs2510923800 | 17:76,200,759 | G/C | — | uncertain significance |
| rs756880800 | 17:76,200,805 | A/G | — | uncertain significance |
| rs750145910 | 17:76,200,807 | G/A | — | uncertain significance |
| rs1263097600 | 17:76,200,912 | C/A | — | uncertain significance |
| rs764562456 | 17:76,200,921 | A/G | — | uncertain significance |
| rs778899836 | 17:76,200,932 | C/A | — | uncertain significance |
| rs72897843 | 17:76,200,965 | C/G | missense variant | — |
| rs200064003 | 17:76,201,226 | C/T | — | uncertain significance |
| rs760754291 | 17:76,201,532 | G/C | — | uncertain significance |
| rs779472218 | 17:76,201,562 | G/A | — | likely benign |
| rs754536494 | 17:76,201,568 | A/G | — | uncertain significance |
| rs141538162 | 17:76,201,573 | A/G | — | likely benign |
| rs139420093 | 17:76,201,734 | C/T | — | uncertain significance |
| rs532591411 | 17:76,201,752 | G/A | — | uncertain significance |
| rs780408595 | 17:76,201,766 | G/A | — | uncertain significance |
| rs781275910 | 17:76,201,779 | A/T | — | uncertain significance |
| rs2510926534 | 17:76,202,043 | A/G | — | likely benign |
| rs756619887 | 17:76,202,083 | C/G | — | uncertain significance |
| rs1480685331 | 17:76,202,090 | A/G | — | uncertain significance |
| rs1026812271 | 17:76,202,107 | C/T | — | likely benign |
| rs745657671 | 17:76,202,119 | C/A | — | uncertain significance |
| rs139832719 | 17:76,202,120 | G/A | — | uncertain significance |
| rs2510926726 | 17:76,202,129 | C/G | — | uncertain significance |
| rs114080902 | 17:76,202,817 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.