HSPA12B
heat shock protein family A (Hsp70) member 12B
Summary
The protein encoded by this gene contains an atypical heat shock protein 70 (Hsp70) ATPase domain and is therefore a distant member of the mammalian Hsp70 family. This gene may be involved in susceptibility to atherosclerosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79285051 | 20:3,715,755 | G/A | intron variant | — |
| rs577327207 | 20:3,721,477 | G/A | — | uncertain significance |
| rs867494918 | 20:3,721,480 | C/T | — | uncertain significance |
| rs34414870 | 20:3,721,485 | G/C | — | benign |
| rs142216650 | 20:3,721,488 | C/G | — | uncertain significance |
| rs556212057 | 20:3,721,507 | C/T | — | uncertain significance |
| rs375250880 | 20:3,721,527 | G/A | — | uncertain significance |
| rs200790194 | 20:3,721,534 | C/T | — | uncertain significance |
| rs375993303 | 20:3,721,545 | C/A | — | uncertain significance |
| rs370476993 | 20:3,722,941 | T/C | — | likely benign |
| rs1310609752 | 20:3,722,944 | G/A | — | uncertain significance |
| rs1303380400 | 20:3,722,962 | C/T | — | uncertain significance |
| rs564348370 | 20:3,725,559 | G/A | — | uncertain significance |
| rs2515066758 | 20:3,725,590 | C/T | — | uncertain significance |
| rs374372742 | 20:3,725,592 | C/G | — | uncertain significance |
| rs2088268852 | 20:3,725,593 | C/T | — | uncertain significance |
| rs145359439 | 20:3,725,633 | C/T | — | likely benign |
| rs1162808467 | 20:3,725,694 | C/T | — | uncertain significance |
| rs200056447 | 20:3,725,707 | A/T | — | uncertain significance |
| rs1183950593 | 20:3,726,584 | C/T | — | uncertain significance |
| rs2515074694 | 20:3,726,634 | T/C | — | uncertain significance |
| rs202158595 | 20:3,726,643 | C/T | — | uncertain significance |
| rs150573779 | 20:3,728,939 | C/T | — | uncertain significance |
| rs139568860 | 20:3,728,949 | G/A | — | uncertain significance |
| rs143974404 | 20:3,729,910 | C/T | synonymous variant | — |
| rs763936271 | 20:3,729,912 | G/A | — | uncertain significance |
| rs758685794 | 20:3,729,961 | A/T | — | uncertain significance |
| rs1331899459 | 20:3,730,403 | G/A | — | uncertain significance |
| rs6139196 | 20:3,730,654 | G/C | — | uncertain significance |
| rs1440779599 | 20:3,730,681 | G/A | — | uncertain significance |
| rs757855596 | 20:3,730,760 | G/A | — | uncertain significance |
| rs748187474 | 20:3,730,787 | C/A | — | uncertain significance |
| rs1489090547 | 20:3,730,838 | G/A | — | uncertain significance |
| rs757023154 | 20:3,730,867 | A/G | — | uncertain significance |
| rs552902059 | 20:3,731,483 | T/C | — | uncertain significance |
| rs2088406312 | 20:3,731,501 | A/G | — | uncertain significance |
| rs771677044 | 20:3,731,512 | G/A | — | uncertain significance |
| rs772562699 | 20:3,731,514 | G/C | — | uncertain significance |
| rs148249749 | 20:3,731,529 | C/A | — | likely benign |
| rs972056637 | 20:3,732,248 | T/G | — | uncertain significance |
| rs2515111898 | 20:3,732,295 | G/A | — | uncertain significance |
| rs563413970 | 20:3,732,298 | G/A | — | uncertain significance |
| rs2515113904 | 20:3,732,481 | T/C | — | uncertain significance |
| rs1281594807 | 20:3,732,607 | A/C | — | uncertain significance |
| rs2515115473 | 20:3,732,622 | G/A | — | uncertain significance |
| rs2088434945 | 20:3,732,650 | A/T | — | uncertain significance |
| rs1429255634 | 20:3,732,666 | C/A | — | likely benign |
| rs1730036330 | 20:3,732,710 | T/C | — | uncertain significance |
| rs368204979 | 20:3,732,718 | G/A | — | uncertain significance |
| rs938733280 | 20:3,732,752 | C/T | — | uncertain significance |
| rs753288533 | 20:3,732,757 | G/A | — | uncertain significance |
| rs948712651 | 20:3,732,773 | A/G | — | uncertain significance |
| rs1417691556 | 20:3,732,787 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.