SAMD15
sterile alpha motif domain containing 15
Summary
Predicted to enable protein serine/threonine kinase activator activity. Predicted to be involved in signal transduction. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368880585 | 14:77,843,771 | G/T | — | uncertain significance |
| rs2503527648 | 14:77,843,790 | C/G | — | uncertain significance |
| rs1421067568 | 14:77,843,871 | C/T | — | uncertain significance |
| rs779375285 | 14:77,843,873 | G/A | — | uncertain significance |
| rs1893856612 | 14:77,843,891 | G/T | — | uncertain significance |
| rs747132452 | 14:77,843,895 | C/T | — | uncertain significance |
| rs61729313 | 14:77,843,920 | A/G | synonymous variant | — |
| rs775931520 | 14:77,843,931 | C/T | — | uncertain significance |
| rs371015537 | 14:77,843,982 | A/T | — | uncertain significance |
| rs2503528364 | 14:77,844,017 | G/A | — | uncertain significance |
| rs1284802469 | 14:77,844,047 | C/T | — | likely benign |
| rs2503528453 | 14:77,844,050 | A/G | — | uncertain significance |
| rs371745458 | 14:77,844,113 | T/G | — | uncertain significance |
| rs769879058 | 14:77,844,137 | A/G | — | likely benign |
| rs369452640 | 14:77,844,285 | C/G | — | uncertain significance |
| rs2503529330 | 14:77,844,363 | A/G | — | uncertain significance |
| rs2503529631 | 14:77,844,473 | C/T | — | uncertain significance |
| rs766095238 | 14:77,844,519 | G/C | — | uncertain significance |
| rs747476384 | 14:77,844,554 | C/A | — | uncertain significance |
| rs145730565 | 14:77,844,610 | G/C | — | uncertain significance |
| rs1277956337 | 14:77,844,626 | C/G | — | uncertain significance |
| rs141415666 | 14:77,844,681 | G/A | — | likely benign |
| rs771582137 | 14:77,844,697 | T/G | — | likely benign |
| rs146296291 | 14:77,844,938 | G/A | — | uncertain significance |
| rs749881791 | 14:77,845,086 | G/A | — | uncertain significance |
| rs141444954 | 14:77,845,176 | T/C | — | uncertain significance |
| rs148358741 | 14:77,845,283 | G/A | — | uncertain significance |
| rs908791333 | 14:77,845,296 | A/G | — | uncertain significance |
| rs150125715 | 14:77,845,790 | G/A | upstream gene variant | — |
| rs2503534640 | 14:77,846,762 | C/T | — | uncertain significance |
| rs4903577 | 14:77,847,258 | C/T | upstream gene variant | — |
| rs7150718 | 14:77,848,618 | G/T | — | — |
| rs4899652 | 14:77,848,972 | A/G | intron variant | — |
| rs4903580 | 14:77,850,978 | C/T | intron variant | — |
| rs1465078129 | 14:77,857,370 | A/G | — | likely benign |
| rs200429320 | 14:77,857,375 | C/T | — | uncertain significance |
| rs149116567 | 14:77,857,405 | C/T | — | uncertain significance |
| rs2503546360 | 14:77,857,439 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.