AS3MT
arsenite methyltransferase
Summary
AS3MT catalyzes the transfer of a methyl group from S-adenosyl-L-methionine (AdoMet) to trivalent arsenical and may play a role in arsenic metabolism (Lin et al., 2002 [PubMed 11790780]).[supplied by OMIM, Mar 2008]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7085104 | 10:104,628,873 | A/G | downstream gene variant | — |
| rs12416687 | 10:104,629,011 | T/C | regulatory region variant | — |
| rs3740400 | 10:104,629,465 | T/G | regulatory region variant | — |
| rs17880345 | 10:104,629,831 | G/T | — | benign |
| rs17878846 | 10:104,630,412 | A/T | downstream gene variant | — |
| rs10786718 | 10:104,631,189 | G/T | — | — |
| rs2493294723 | 10:104,632,254 | A/G | — | uncertain significance |
| rs772572895 | 10:104,632,288 | G/T | — | uncertain significance |
| rs764428592 | 10:104,632,345 | C/G | — | uncertain significance |
| rs200488263 | 10:104,632,881 | T/C | — | uncertain significance |
| rs767695284 | 10:104,632,887 | A/G | — | uncertain significance |
| rs7920657 | 10:104,633,244 | T/G | — | — |
| rs12764899 | 10:104,635,103 | G/C | — | — |
| rs12765002 | 10:104,635,348 | C/G | — | — |
| rs3740393 | 10:104,636,655 | G/T | — | — |
| rs576986384 | 10:104,636,738 | G/A | — | uncertain significance |
| rs3740392 | 10:104,636,855 | T/C | intron variant | — |
| rs11191434 | 10:104,637,508 | T/C | intron variant | — |
| rs11191438 | 10:104,637,864 | G/A | — | — |
| rs1564791785 | 10:104,638,147 | G/A | — | uncertain significance |
| rs531874964 | 10:104,638,186 | C/A | — | uncertain significance |
| rs3740390 | 10:104,638,480 | C/T | intron variant | — |
| rs1238646346 | 10:104,638,681 | T/C | — | uncertain significance |
| rs1311891557 | 10:104,638,698 | A/G | — | uncertain significance |
| rs11191439 | 10:104,638,723 | T/A | missense variant | — |
| rs202100735 | 10:104,642,847 | A/T | — | — |
| rs11191442 | 10:104,643,596 | T/A | downstream gene variant | — |
| rs7100709 | 10:104,649,729 | A/C | upstream gene variant | — |
| rs202060999 | 10:104,650,365 | A/G | — | uncertain significance |
| rs1424241173 | 10:104,650,377 | T/C | — | uncertain significance |
| rs928210555 | 10:104,650,386 | T/C | — | uncertain significance |
| rs11191447 | 10:104,652,323 | C/T | upstream gene variant | — |
| rs10786721 | 10:104,654,383 | C/A | intron variant | — |
| rs113282265 | 10:104,657,248 | A/T | — | — |
| rs12218148 | 10:104,657,469 | C/A | intron variant | — |
| rs7909591 | 10:104,659,018 | G/T | intron variant | — |
| rs11191454 | 10:104,660,004 | A/G | intron variant | — |
| rs10748835 | 10:104,660,256 | G/A | intron variant | — |
| rs777235719 | 10:104,660,363 | A/G | — | uncertain significance |
| rs17884001 | 10:104,661,245 | C/T | regulatory region variant | — |
| rs1046778 | 10:104,661,484 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.