MAPK12
mitogen-activated protein kinase 12
Summary
Activation of members of the mitogen-activated protein kinase family is a major mechanism for transduction of extracellular signals. Stress-activated protein kinases are one subclass of MAP kinases. The protein encoded by this gene functions as a signal transducer during differentiation of myoblasts to myotubes. [provided by RefSeq, Jul 2008]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs562826406 | 22:50,691,903 | G/C | — | uncertain significance |
| rs181718127 | 22:50,693,474 | C/A | upstream gene variant | — |
| rs773024220 | 22:50,693,653 | C/T | — | uncertain significance |
| rs555010998 | 22:50,693,670 | T/G | — | uncertain significance |
| rs139984390 | 22:50,693,673 | T/C | — | uncertain significance |
| rs149438446 | 22:50,693,695 | C/A | — | uncertain significance |
| rs201016559 | 22:50,693,697 | T/C | — | uncertain significance |
| rs770945104 | 22:50,693,707 | G/A | — | uncertain significance |
| rs775287258 | 22:50,693,716 | C/T | — | uncertain significance |
| rs559897016 | 22:50,693,724 | G/A | — | uncertain significance |
| rs200947001 | 22:50,693,754 | C/T | — | uncertain significance |
| rs368005916 | 22:50,693,950 | T/C | — | uncertain significance |
| rs1231217204 | 22:50,694,049 | C/T | — | uncertain significance |
| rs2519278078 | 22:50,694,069 | A/G | — | uncertain significance |
| rs371441235 | 22:50,694,522 | G/A | — | uncertain significance |
| rs138065172 | 22:50,694,528 | C/T | — | likely benign |
| rs541009038 | 22:50,694,558 | C/T | — | uncertain significance |
| rs112567753 | 22:50,694,567 | C/T | — | uncertain significance |
| rs149914576 | 22:50,694,568 | G/A | — | uncertain significance |
| rs374797423 | 22:50,695,063 | C/T | — | uncertain significance |
| rs150223264 | 22:50,695,552 | G/A | — | uncertain significance |
| rs143887978 | 22:50,695,816 | G/A | intron variant | — |
| rs767106347 | 22:50,699,606 | C/T | — | uncertain significance |
| rs368055751 | 22:50,699,645 | T/A | — | uncertain significance |
| rs558276175 | 22:50,699,669 | G/A | — | conflicting classifications of pathogenicity |
| rs771733687 | 22:50,699,672 | C/G | — | uncertain significance |
| rs2065210637 | 22:50,699,702 | C/T | — | uncertain significance |
| rs1244376929 | 22:50,699,842 | C/T | — | uncertain significance |
| rs772106264 | 22:50,699,844 | G/A | — | uncertain significance |
| rs776449594 | 22:50,699,868 | C/T | — | uncertain significance |
| rs1465168100 | 22:50,699,901 | C/A | — | uncertain significance |
| rs2519294825 | 22:50,699,910 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.