SULT1A2
sulfotransferase family 1A member 2
Summary
Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes one of two phenol sulfotransferases with thermostable enzyme activity. Two alternatively spliced variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs577093363 | 16:28,603,363 | G/A | — | uncertain significance |
| rs776571529 | 16:28,603,395 | G/A | — | uncertain significance |
| rs376675029 | 16:28,603,414 | G/A | — | uncertain significance |
| rs2506788947 | 16:28,603,422 | T/C | — | uncertain significance |
| rs200765354 | 16:28,603,429 | C/T | — | uncertain significance |
| rs2506792193 | 16:28,603,621 | C/G | — | uncertain significance |
| rs772334533 | 16:28,603,625 | C/T | — | likely benign |
| rs145465524 | 16:28,603,628 | C/T | — | uncertain significance |
| rs200128334 | 16:28,603,722 | G/A | — | uncertain significance |
| rs183030982 | 16:28,603,725 | C/T | — | uncertain significance |
| rs1262885746 | 16:28,603,743 | T/C | — | uncertain significance |
| rs2506804823 | 16:28,604,574 | T/A | — | uncertain significance |
| rs778431880 | 16:28,604,575 | C/T | — | uncertain significance |
| rs749565589 | 16:28,604,602 | G/T | — | uncertain significance |
| rs191186879 | 16:28,604,641 | C/T | — | uncertain significance |
| rs767576971 | 16:28,604,658 | C/G | — | uncertain significance |
| rs2506806592 | 16:28,604,664 | G/A | — | uncertain significance |
| rs891602583 | 16:28,604,665 | A/G | — | uncertain significance |
| rs3743963 | 16:28,604,686 | A/G | downstream gene variant | — |
| rs2506809087 | 16:28,604,775 | T/C | — | uncertain significance |
| rs2047021992 | 16:28,604,813 | G/C | — | uncertain significance |
| rs764148152 | 16:28,604,817 | A/G | — | likely benign |
| rs1298621535 | 16:28,604,819 | A/G | — | uncertain significance |
| rs369978676 | 16:28,604,821 | T/G | — | uncertain significance |
| rs374846262 | 16:28,604,868 | C/T | — | uncertain significance |
| rs1157807975 | 16:28,606,720 | G/A | — | uncertain significance |
| rs530005107 | 16:28,606,764 | G/T | — | uncertain significance |
| rs770776557 | 16:28,606,780 | C/T | — | uncertain significance |
| rs759963275 | 16:28,606,931 | G/C | — | uncertain significance |
| rs148980876 | 16:28,606,952 | C/T | — | uncertain significance |
| rs4149406 | 16:28,607,070 | A/G | downstream gene variant | — |
| rs141979421 | 16:28,607,106 | G/A | — | uncertain significance |
| rs72791898 | 16:28,609,592 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.