MAST4
microtubule associated serine/threonine kinase family member 4
Summary
This gene encodes a member of the microtubule-associated serine/threonine protein kinases. The proteins in this family contain a domain that gives the kinase the ability to determine its own scaffold to control the effects of their kinase activities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
Known Variants168 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201236388 | 5:65,892,523 | C/T | — | uncertain significance |
| rs1274035672 | 5:65,892,584 | C/T | — | uncertain significance |
| rs546671806 | 5:65,892,819 | C/T | — | likely benign |
| rs62362269 | 5:65,906,379 | C/T | intron variant | — |
| rs13190235 | 5:65,964,783 | T/A | — | — |
| rs60613433 | 5:65,969,162 | G/A | intron variant | — |
| rs61707595 | 5:66,001,101 | A/G | regulatory region variant | — |
| rs59596869 | 5:66,006,325 | C/T | intron variant | — |
| rs565434858 | 5:66,055,563 | C/T | — | benign |
| rs200785678 | 5:66,055,573 | C/T | — | likely benign |
| rs6864743 | 5:66,055,656 | G/A | — | benign |
| rs1423642 | 5:66,100,540 | A/T | — | — |
| rs57246240 | 5:66,112,715 | G/A | intron variant | — |
| rs55929615 | 5:66,113,064 | G/A | — | — |
| rs56403004 | 5:66,115,539 | G/A | — | — |
| rs747442997 | 5:66,124,697 | G/A | — | uncertain significance |
| rs981480743 | 5:66,140,080 | C/T | — | uncertain significance |
| rs39861 | 5:66,152,258 | A/G | intron variant | — |
| rs1972739 | 5:66,160,022 | G/A | — | — |
| rs154619 | 5:66,200,447 | A/G | — | — |
| rs27218 | 5:66,207,261 | T/G | — | — |
| rs250277 | 5:66,314,241 | A/G | intron variant | — |
| rs6889240 | 5:66,320,940 | A/G | intron variant | — |
| rs1226140923 | 5:66,350,237 | G/A | — | uncertain significance |
| rs773838694 | 5:66,350,249 | G/A | — | uncertain significance |
| rs2530790139 | 5:66,350,252 | A/G | — | uncertain significance |
| rs2531474121 | 5:66,391,499 | T/G | — | uncertain significance |
| rs1764912143 | 5:66,396,328 | C/G | — | uncertain significance |
| rs1764912884 | 5:66,396,338 | A/G | — | uncertain significance |
| rs566036999 | 5:66,396,368 | A/G | — | uncertain significance |
| rs563420885 | 5:66,398,372 | G/A | — | uncertain significance |
| rs575099215 | 5:66,398,393 | A/G | — | uncertain significance |
| rs763876338 | 5:66,400,245 | C/A | — | uncertain significance |
| rs775033679 | 5:66,400,356 | C/G | — | uncertain significance |
| rs371642698 | 5:66,400,357 | G/A | — | uncertain significance |
| rs200689112 | 5:66,405,916 | T/C | — | likely benign |
| rs2531689722 | 5:66,405,929 | C/T | — | uncertain significance |
| rs375943354 | 5:66,405,955 | G/T | — | uncertain significance |
| rs2531690647 | 5:66,405,975 | T/C | — | uncertain significance |
| rs758695119 | 5:66,406,010 | C/T | — | uncertain significance |
| rs756149069 | 5:66,409,982 | G/T | — | uncertain significance |
| rs554135142 | 5:66,414,554 | C/A | — | uncertain significance |
| rs769608347 | 5:66,416,851 | A/G | — | uncertain significance |
| rs371467835 | 5:66,416,870 | G/A | — | uncertain significance |
| rs755939508 | 5:66,416,924 | C/G | — | uncertain significance |
| rs780078957 | 5:66,416,927 | A/G | — | uncertain significance |
| rs753723805 | 5:66,426,069 | C/T | — | uncertain significance |
| rs56269713 | 5:66,427,729 | G/A | — | benign |
| rs748171577 | 5:66,427,751 | A/G | — | uncertain significance |
| rs368570489 | 5:66,429,367 | A/G | — | uncertain significance |
| rs768415374 | 5:66,437,974 | C/G | — | uncertain significance |
| rs772506443 | 5:66,437,987 | G/A | — | uncertain significance |
| rs367759530 | 5:66,438,315 | A/G | — | uncertain significance |
| rs2532194146 | 5:66,438,324 | T/C | — | likely pathogenic |
| rs1770852782 | 5:66,440,539 | G/A | — | uncertain significance |
| rs78130987 | 5:66,441,149 | C/G | — | likely benign |
| rs200645819 | 5:66,445,265 | G/A | — | uncertain significance |
| rs376798686 | 5:66,445,309 | G/A | — | uncertain significance |
| rs779542474 | 5:66,445,340 | G/C | — | uncertain significance |
| rs768246590 | 5:66,448,468 | T/C | — | uncertain significance |
| rs765442001 | 5:66,448,537 | G/A | — | uncertain significance |
| rs149652400 | 5:66,448,560 | T/A | — | conflicting classifications of pathogenicity |
| rs754657959 | 5:66,448,591 | C/T | — | uncertain significance |
| rs748456473 | 5:66,448,594 | T/C | — | uncertain significance |
| rs77194622 | 5:66,448,644 | C/T | — | likely pathogenic |
| rs367798348 | 5:66,448,668 | A/T | — | uncertain significance |
| rs371209983 | 5:66,448,688 | C/T | — | likely benign |
| rs1342348159 | 5:66,449,283 | T/C | — | uncertain significance |
| rs56383960 | 5:66,449,305 | C/T | — | likely benign |
| rs201669513 | 5:66,449,326 | A/G | — | uncertain significance |
| rs199850727 | 5:66,449,356 | G/A | — | uncertain significance |
| rs1697137 | 5:66,452,175 | G/A | intron variant | — |
| rs1023036855 | 5:66,458,482 | T/C | — | uncertain significance |
| rs2532499908 | 5:66,458,562 | T/G | — | uncertain significance |
| rs201605726 | 5:66,458,571 | C/G | — | uncertain significance |
| rs2532510272 | 5:66,459,019 | A/G | — | uncertain significance |
| rs1561196461 | 5:66,459,078 | A/T | — | uncertain significance |
| rs368420355 | 5:66,459,103 | G/A | — | uncertain significance |
| rs200858877 | 5:66,459,234 | C/G | — | uncertain significance |
| rs528251606 | 5:66,459,244 | T/C | — | likely benign |
| rs901676378 | 5:66,459,415 | G/A | — | uncertain significance |
| rs2532519592 | 5:66,459,419 | C/T | — | uncertain significance |
| rs372874851 | 5:66,459,471 | C/A | — | uncertain significance |
| rs774911010 | 5:66,459,562 | G/A | — | uncertain significance |
| rs766998132 | 5:66,459,589 | G/A | — | uncertain significance |
| rs1166383218 | 5:66,459,632 | A/G | — | uncertain significance |
| rs751749924 | 5:66,459,810 | C/A | — | uncertain significance |
| rs201670700 | 5:66,459,842 | G/A | — | uncertain significance |
| rs200132752 | 5:66,459,843 | C/A | — | uncertain significance |
| rs1296853806 | 5:66,459,920 | G/A | — | uncertain significance |
| rs751115486 | 5:66,459,937 | A/G | — | uncertain significance |
| rs375341543 | 5:66,460,160 | T/C | — | uncertain significance |
| rs779290997 | 5:66,460,174 | G/A | — | uncertain significance |
| rs758768683 | 5:66,460,237 | A/G | — | uncertain significance |
| rs1341001081 | 5:66,460,273 | G/A | — | uncertain significance |
| rs202199042 | 5:66,460,279 | C/T | — | uncertain significance |
| rs747857936 | 5:66,460,385 | G/A | — | uncertain significance |
| rs766409259 | 5:66,460,469 | C/T | — | likely benign |
| rs376616827 | 5:66,460,505 | G/A | — | uncertain significance |
| rs201907198 | 5:66,460,561 | G/C | — | uncertain significance |
Showing 100 of 168 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.