MAPKAP1
MAPK associated protein 1
Summary
This gene encodes a protein that is highly similar to the yeast SIN1 protein, a stress-activated protein kinase. Alternatively spliced transcript variants encoding distinct isoforms have been described. Alternate polyadenylation sites as well as alternate 3' UTRs have been identified for transcripts of this gene. [provided by RefSeq, Jul 2008]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1441208408 | 9:128,201,224 | T/G | — | uncertain significance |
| rs111458512 | 9:128,201,271 | C/T | — | benign |
| rs555771876 | 9:128,206,796 | T/C | — | uncertain significance |
| rs35549826 | 9:128,206,855 | C/T | — | benign |
| rs752861508 | 9:128,206,869 | T/C | — | uncertain significance |
| rs199955511 | 9:128,221,686 | C/T | — | — |
| rs10986769 | 9:128,222,340 | A/T | — | — |
| rs2541780874 | 9:128,230,325 | C/A | — | uncertain significance |
| rs10121005 | 9:128,252,604 | A/G | intron variant | — |
| rs1357279093 | 9:128,268,636 | G/C | — | uncertain significance |
| rs11542134 | 9:128,305,390 | T/C | — | benign |
| rs536861 | 9:128,313,444 | A/C | intron variant | — |
| rs1830838274 | 9:128,322,020 | G/A | — | uncertain significance |
| rs13294217 | 9:128,326,190 | C/T | upstream gene variant | — |
| rs377752331 | 9:128,347,904 | C/T | — | uncertain significance |
| rs757433296 | 9:128,347,973 | C/G | — | uncertain significance |
| rs12554256 | 9:128,385,423 | G/T | — | — |
| rs473426 | 9:128,406,988 | C/G | — | benign |
| rs376993327 | 9:128,420,018 | C/G | — | uncertain significance |
| rs2538318247 | 9:128,420,055 | C/T | — | uncertain significance |
| rs4838281 | 9:128,431,502 | G/A | intron variant | — |
| rs201151787 | 9:128,434,756 | T/C | — | uncertain significance |
| rs2538354205 | 9:128,434,759 | A/G | — | uncertain significance |
| rs142713473 | 9:128,434,806 | C/T | — | likely benign |
| rs144290254 | 9:128,434,810 | C/T | — | uncertain significance |
| rs1403717933 | 9:128,434,823 | G/C | — | uncertain significance |
| rs148740501 | 9:128,434,832 | T/C | — | uncertain significance |
| rs77961302 | 9:128,451,741 | A/C | — | — |
| rs13296765 | 9:128,455,859 | T/C | intron variant | — |
| rs138286128 | 9:128,455,969 | T/C | — | — |
| rs62567183 | 9:128,456,117 | T/C | — | — |
| rs752493195 | 9:128,468,344 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.