MAP3K19
mitogen-activated protein kinase kinase kinase 19
Summary
Predicted to enable ATP binding activity; protein serine kinase activity; and protein serine/threonine kinase activity. Predicted to be involved in MAPK cascade. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778077139 | 2:135,722,445 | T/C | — | uncertain significance |
| rs150711518 | 2:135,722,480 | C/G | — | uncertain significance |
| rs113529902 | 2:135,725,663 | C/T | regulatory region variant | — |
| rs374688821 | 2:135,726,704 | G/A | — | — |
| rs760518747 | 2:135,738,407 | G/A | — | uncertain significance |
| rs373039984 | 2:135,738,463 | C/T | — | uncertain significance |
| rs779120521 | 2:135,738,473 | C/T | — | uncertain significance |
| rs536503445 | 2:135,738,521 | T/C | — | uncertain significance |
| rs763964181 | 2:135,738,802 | A/G | — | uncertain significance |
| rs2467742808 | 2:135,738,809 | T/C | — | uncertain significance |
| rs1302328314 | 2:135,738,977 | C/T | — | uncertain significance |
| rs766757166 | 2:135,741,251 | C/T | — | uncertain significance |
| rs55832179 | 2:135,741,367 | T/C | — | uncertain significance |
| rs1685058107 | 2:135,743,470 | A/G | — | uncertain significance |
| rs554230531 | 2:135,743,503 | A/G | — | uncertain significance |
| rs752609319 | 2:135,743,573 | T/C | — | uncertain significance |
| rs769741999 | 2:135,743,637 | C/G | — | uncertain significance |
| rs373734617 | 2:135,743,813 | A/T | — | uncertain significance |
| rs2467783950 | 2:135,743,835 | C/A | — | uncertain significance |
| rs2467784610 | 2:135,743,881 | T/C | — | uncertain significance |
| rs761136736 | 2:135,744,016 | A/G | — | uncertain significance |
| rs142728110 | 2:135,744,019 | G/C | — | uncertain significance |
| rs1335764025 | 2:135,744,074 | G/C | — | uncertain significance |
| rs771588420 | 2:135,744,137 | T/C | — | uncertain significance |
| rs147328989 | 2:135,744,271 | T/G | — | uncertain significance |
| rs2467791022 | 2:135,744,347 | T/C | — | uncertain significance |
| rs1276659088 | 2:135,744,385 | C/T | — | uncertain significance |
| rs148647253 | 2:135,744,386 | G/A | — | uncertain significance |
| rs1319473383 | 2:135,744,402 | A/C | — | uncertain significance |
| rs776326821 | 2:135,744,423 | A/T | — | uncertain significance |
| rs372722964 | 2:135,744,509 | T/C | — | uncertain significance |
| rs746373900 | 2:135,744,556 | G/A | — | uncertain significance |
| rs200920212 | 2:135,744,628 | C/T | — | likely benign |
| rs752221342 | 2:135,744,629 | G/A | — | uncertain significance |
| rs373802326 | 2:135,744,718 | G/A | — | uncertain significance |
| rs1194382006 | 2:135,744,776 | T/C | — | uncertain significance |
| rs1477040353 | 2:135,744,797 | G/T | — | uncertain significance |
| rs748308749 | 2:135,744,823 | G/A | — | uncertain significance |
| rs1353471825 | 2:135,744,895 | T/C | — | uncertain significance |
| rs199849486 | 2:135,745,024 | C/T | — | uncertain significance |
| rs767794263 | 2:135,745,033 | A/G | — | likely benign |
| rs1038421124 | 2:135,745,132 | C/A | — | uncertain significance |
| rs1217570856 | 2:135,745,160 | T/A | — | uncertain significance |
| rs756014611 | 2:135,745,171 | T/A | — | uncertain significance |
| rs2467804026 | 2:135,745,282 | A/G | — | uncertain significance |
| rs766460495 | 2:135,745,655 | C/T | — | likely benign |
| rs2467811416 | 2:135,745,762 | T/C | — | likely benign |
| rs2467811434 | 2:135,745,763 | T/C | — | uncertain significance |
| rs1282444278 | 2:135,756,356 | T/C | — | uncertain significance |
| rs1686215732 | 2:135,756,385 | A/G | — | uncertain significance |
| rs756100551 | 2:135,756,490 | A/C | — | uncertain significance |
| rs145950712 | 2:135,756,510 | A/G | — | likely benign |
| rs769086800 | 2:135,756,538 | G/A | — | uncertain significance |
| rs4954218 | 2:135,803,425 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.