STK11
serine/threonine kinase 11
Summary
The protein encoded by this gene is a serine/threonine kinase that regulates cell polarity and energy metabolism and functions as a tumor suppressor. Mutations in this gene have been associated with the autosomal dominant Peutz-Jeghers syndrome, as well as with skin, pancreatic, and testicular cancers. [provided by RefSeq, May 2022]
Known Variants1,501 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs185744805 | 19:1,201,925 | G/A | — | likely benign |
| rs759197411 | 19:1,205,343 | G/C | — | likely benign |
| rs114497905 | 19:1,205,490 | A/G | — | likely benign |
| rs74720037 | 19:1,205,637 | T/G | — | benign |
| rs886054201 | 19:1,205,815 | G/A | — | uncertain significance |
| rs944606544 | 19:1,205,816 | G/T | — | uncertain significance |
| rs886054202 | 19:1,205,858 | C/T | — | uncertain significance |
| rs147615524 | 19:1,205,889 | C/T | regulatory region variant | benign |
| rs886054203 | 19:1,205,988 | C/T | — | uncertain significance |
| rs867696290 | 19:1,206,020 | C/T | — | uncertain significance |
| rs1169622696 | 19:1,206,078 | C/T | — | uncertain significance |
| rs1368940227 | 19:1,206,107 | C/T | — | uncertain significance |
| rs2080662705 | 19:1,206,130 | G/A | — | uncertain significance |
| rs868538577 | 19:1,206,138 | G/A | — | uncertain significance |
| rs1388166210 | 19:1,206,139 | C/T | — | uncertain significance |
| rs886054204 | 19:1,206,190 | G/T | — | uncertain significance |
| rs1050439702 | 19:1,206,323 | C/T | — | uncertain significance |
| rs886054206 | 19:1,206,326 | G/C | — | uncertain significance |
| rs548605358 | 19:1,206,333 | G/A | — | benign |
| rs560480063 | 19:1,206,336 | C/T | — | benign |
| rs187649480 | 19:1,206,351 | G/C | — | benign |
| rs1316450313 | 19:1,206,362 | C/T | — | likely benign |
| rs886054207 | 19:1,206,367 | G/A | — | uncertain significance |
| rs886054208 | 19:1,206,393 | C/T | — | uncertain significance |
| rs866050909 | 19:1,206,439 | G/A | — | uncertain significance |
| rs552610464 | 19:1,206,452 | G/A | — | conflicting classifications of pathogenicity |
| rs867231569 | 19:1,206,466 | C/T | — | uncertain significance |
| rs115594813 | 19:1,206,483 | C/T | — | likely benign |
| rs2080666270 | 19:1,206,525 | C/T | — | uncertain significance |
| rs886054209 | 19:1,206,526 | C/T | — | uncertain significance |
| rs1208293548 | 19:1,206,580 | G/T | — | uncertain significance |
| rs149756065 | 19:1,206,602 | C/T | — | likely benign |
| rs935371253 | 19:1,206,611 | G/A | — | uncertain significance |
| rs893914050 | 19:1,206,633 | C/A | — | likely benign |
| rs372994361 | 19:1,206,639 | C/T | — | benign |
| rs886054210 | 19:1,206,684 | C/G | — | uncertain significance |
| rs886054211 | 19:1,206,697 | A/C | — | uncertain significance |
| rs561818770 | 19:1,206,720 | C/G | — | uncertain significance |
| rs1273032629 | 19:1,206,746 | C/T | — | likely benign |
| rs1453851790 | 19:1,206,763 | G/A | — | uncertain significance |
| rs527710714 | 19:1,206,776 | C/T | — | likely benign |
| rs777480684 | 19:1,206,777 | C/T | — | uncertain significance |
| rs1340865672 | 19:1,206,785 | G/T | — | uncertain significance |
| rs532196225 | 19:1,206,786 | T/C | — | likely benign |
| rs886054213 | 19:1,206,807 | C/T | — | uncertain significance |
| rs1407068597 | 19:1,206,814 | C/T | — | likely benign |
| rs1323638467 | 19:1,206,818 | G/T | — | likely benign |
| rs886054214 | 19:1,206,832 | A/G | — | uncertain significance |
| rs886054215 | 19:1,206,858 | C/T | — | uncertain significance |
| rs549974432 | 19:1,206,864 | A/C | — | benign |
| rs1044460918 | 19:1,206,865 | C/G | — | likely benign |
| rs1057522370 | 19:1,206,894 | C/T | — | likely benign |
| rs1555734829 | 19:1,206,896 | A/G | — | likely benign |
| rs1568689691 | 19:1,206,897 | G/A | — | likely benign |
| rs2145404308 | 19:1,206,901 | C/T | — | likely benign |
| rs772584871 | 19:1,206,902 | C/T | — | likely benign |
| rs748868995 | 19:1,206,903 | T/G | — | likely benign |
| rs770466669 | 19:1,206,904 | G/A | — | conflicting classifications of pathogenicity |
| rs2080669573 | 19:1,206,907 | T/A | — | uncertain significance |
| rs786203043 | 19:1,206,908 | C/T | — | uncertain significance |
| rs1181075160 | 19:1,206,909 | C/T | — | uncertain significance |
| rs774072752 | 19:1,206,911 | G/T | — | conflicting classifications of pathogenicity |
| rs759284466 | 19:1,206,912 | C/T | — | conflicting classifications of pathogenicity |
| rs2080669644 | 19:1,206,913 | A/T | — | uncertain significance |
| rs1599914695 | 19:1,206,916 | G/C | — | uncertain significance |
| rs1159551738 | 19:1,206,917 | A/C | — | conflicting classifications of pathogenicity |
| rs1271482574 | 19:1,206,918 | G/A | — | likely benign |
| rs906049559 | 19:1,206,919 | G/A | — | uncertain significance |
| rs886054216 | 19:1,206,920 | T/G | — | uncertain significance |
| rs1555734857 | 19:1,206,921 | G/A | — | likely benign |
| rs767300470 | 19:1,206,922 | G/A | — | uncertain significance |
| rs1599914720 | 19:1,206,923 | T/C | — | conflicting classifications of pathogenicity |
| rs1379886566 | 19:1,206,924 | G/A | — | likely benign |
| rs1399081375 | 19:1,206,925 | G/A | — | conflicting classifications of pathogenicity |
| rs1178249537 | 19:1,206,926 | A/G | — | uncertain significance |
| rs786201498 | 19:1,206,927 | C/T | — | conflicting classifications of pathogenicity |
| rs1360284524 | 19:1,206,928 | C/A | — | uncertain significance |
| rs775346785 | 19:1,206,929 | C/G | — | uncertain significance |
| rs1555734869 | 19:1,206,930 | G/C | — | likely benign |
| rs2080669968 | 19:1,206,931 | C/T | — | pathogenic |
| rs2145404457 | 19:1,206,932 | A/G | — | uncertain significance |
| rs760588289 | 19:1,206,934 | C/G | — | uncertain significance |
| rs1379630288 | 19:1,206,936 | G/C | — | conflicting classifications of pathogenicity |
| rs876661079 | 19:1,206,937 | C/G | — | uncertain significance |
| rs764154797 | 19:1,206,938 | T/A | — | uncertain significance |
| rs876659432 | 19:1,206,939 | G/C | — | likely benign |
| rs2145404498 | 19:1,206,940 | G/A | — | uncertain significance |
| rs2080670108 | 19:1,206,941 | G/T | — | uncertain significance |
| rs876660012 | 19:1,206,942 | C/T | — | conflicting classifications of pathogenicity |
| rs753834428 | 19:1,206,943 | A/G | — | uncertain significance |
| rs2145404514 | 19:1,206,944 | T/C | — | uncertain significance |
| rs757411357 | 19:1,206,945 | G/T | — | uncertain significance |
| rs2145404533 | 19:1,206,948 | C/T | — | likely benign |
| rs2145404536 | 19:1,206,949 | A/G | — | uncertain significance |
| rs1599914790 | 19:1,206,950 | C/T | — | uncertain significance |
| rs765330434 | 19:1,206,951 | G/C | — | likely benign |
| rs750708224 | 19:1,206,953 | A/G | — | uncertain significance |
| rs758769888 | 19:1,206,954 | G/T | — | uncertain significance |
| rs1060499970 | 19:1,206,955 | G/A | — | conflicting classifications of pathogenicity |
| rs1458974438 | 19:1,206,956 | G/A | — | uncertain significance |
Showing 100 of 1,501 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.