SERPINA12
serpin family A member 12
Summary
Enables molecular function inhibitor activity. Predicted to act upstream of or within negative regulation of gluconeogenesis; positive regulation of signal transduction; and regulation of lipid metabolic process. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200929043 | 14:94,953,664 | C/A | — | uncertain significance |
| rs1363897458 | 14:94,953,677 | A/G | — | uncertain significance |
| rs1469736427 | 14:94,953,764 | T/C | — | uncertain significance |
| rs138209155 | 14:94,953,767 | G/A | missense variant | — |
| rs780759007 | 14:94,953,771 | C/T | — | uncertain significance |
| rs142812237 | 14:94,953,818 | G/T | — | uncertain significance |
| rs1470474112 | 14:94,953,822 | T/C | — | uncertain significance |
| rs140198372 | 14:94,953,832 | C/A | splice region variant | — |
| rs200583511 | 14:94,953,836 | G/A | splice region variant | — |
| rs1445117727 | 14:94,955,959 | C/A | — | pathogenic |
| rs372459048 | 14:94,955,976 | C/T | — | uncertain significance |
| rs142210723 | 14:94,956,030 | C/T | — | likely benign |
| rs773146990 | 14:94,956,058 | C/T | — | likely benign |
| rs571250364 | 14:94,956,063 | G/A | — | uncertain significance |
| rs1330519693 | 14:94,956,076 | G/A | — | uncertain significance |
| rs1264660783 | 14:94,956,078 | A/T | — | uncertain significance |
| rs1998207 | 14:94,957,714 | G/C | — | — |
| rs181727536 | 14:94,959,093 | G/T | intron variant | — |
| rs2236242 | 14:94,960,052 | T/A | intron variant | — |
| rs143675343 | 14:94,961,918 | C/T | intron variant | — |
| rs143897400 | 14:94,962,714 | G/A | — | benign |
| rs761165782 | 14:94,962,765 | C/T | — | uncertain significance |
| rs372389745 | 14:94,962,792 | G/A | — | uncertain significance |
| rs2503555614 | 14:94,962,807 | C/G | — | uncertain significance |
| rs1900425956 | 14:94,962,813 | T/C | — | uncertain significance |
| rs34827644 | 14:94,962,832 | T/C | — | benign |
| rs779982393 | 14:94,962,839 | A/G | — | uncertain significance |
| rs201400041 | 14:94,962,840 | T/G | — | uncertain significance |
| rs148689361 | 14:94,962,865 | G/A | — | benign |
| rs759753080 | 14:94,962,871 | T/G | — | uncertain significance |
| rs74077729 | 14:94,962,897 | T/C | — | likely benign |
| rs200726648 | 14:94,962,936 | C/A | — | uncertain significance |
| rs752631480 | 14:94,964,103 | C/T | — | uncertain significance |
| rs61757459 | 14:94,964,104 | G/A | stop gained | pathogenic |
| rs61758960 | 14:94,964,127 | A/G | missense variant | — |
| rs1028564772 | 14:94,964,164 | T/C | — | uncertain significance |
| rs148004456 | 14:94,964,247 | A/G | — | uncertain significance |
| rs774278015 | 14:94,964,293 | G/A | — | uncertain significance |
| rs17090972 | 14:94,964,311 | G/T | — | benign |
| rs1056703619 | 14:94,964,358 | T/G | — | uncertain significance |
| rs1223925909 | 14:94,964,362 | G/T | — | uncertain significance |
| rs199680231 | 14:94,964,379 | A/C | — | uncertain significance |
| rs575676262 | 14:94,964,395 | C/T | — | uncertain significance |
| rs1278161134 | 14:94,964,527 | T/C | — | uncertain significance |
| rs780171767 | 14:94,964,530 | C/A | — | uncertain significance |
| rs1285811651 | 14:94,964,607 | A/G | — | uncertain significance |
| rs749001752 | 14:94,964,677 | G/C | — | uncertain significance |
| rs144650232 | 14:94,966,702 | T/A | intron variant | — |
| rs570487320 | 14:94,968,405 | G/C | — | — |
| rs11627075 | 14:94,972,242 | C/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.