MTHFSD
methenyltetrahydrofolate synthetase domain containing
Summary
Enables RNA binding activity. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2507485505 | 16:86,565,631 | G/C | — | uncertain significance |
| rs953140970 | 16:86,565,651 | C/G | — | uncertain significance |
| rs372334535 | 16:86,565,672 | C/A | — | uncertain significance |
| rs752299303 | 16:86,565,673 | G/A | — | uncertain significance |
| rs772148426 | 16:86,565,720 | G/A | — | uncertain significance |
| rs1413964726 | 16:86,565,730 | G/A | — | uncertain significance |
| rs751056359 | 16:86,565,741 | C/T | — | likely benign |
| rs369644027 | 16:86,565,790 | G/A | — | uncertain significance |
| rs142996375 | 16:86,565,823 | C/G | — | uncertain significance |
| rs778077707 | 16:86,565,825 | C/T | — | uncertain significance |
| rs200853025 | 16:86,565,838 | C/T | — | uncertain significance |
| rs781526627 | 16:86,565,877 | G/C | — | uncertain significance |
| rs1192217161 | 16:86,565,879 | G/A | — | uncertain significance |
| rs370582414 | 16:86,565,919 | C/T | — | uncertain significance |
| rs977111695 | 16:86,565,985 | G/T | — | uncertain significance |
| rs776250628 | 16:86,566,024 | C/A | — | uncertain significance |
| rs768632861 | 16:86,575,379 | T/A | — | uncertain significance |
| rs201325688 | 16:86,575,380 | C/G | — | uncertain significance |
| rs769433175 | 16:86,575,721 | C/T | — | uncertain significance |
| rs375640712 | 16:86,575,751 | C/T | — | uncertain significance |
| rs546388135 | 16:86,575,772 | T/C | — | uncertain significance |
| rs372016279 | 16:86,575,787 | C/T | — | uncertain significance |
| rs761453315 | 16:86,575,795 | C/G | — | uncertain significance |
| rs2507663191 | 16:86,575,819 | C/G | — | uncertain significance |
| rs372453466 | 16:86,580,177 | C/T | — | uncertain significance |
| rs199987477 | 16:86,580,242 | T/C | — | uncertain significance |
| rs759604504 | 16:86,582,086 | T/A | — | uncertain significance |
| rs1197397026 | 16:86,582,144 | T/C | — | uncertain significance |
| rs201622566 | 16:86,582,171 | A/C | — | uncertain significance |
| rs781188041 | 16:86,585,641 | G/C | — | uncertain significance |
| rs544568797 | 16:86,585,706 | G/A | — | uncertain significance |
| rs762208272 | 16:86,585,736 | C/G | — | uncertain significance |
| rs2507913262 | 16:86,588,267 | C/T | — | uncertain significance |
| rs555087275 | 16:86,588,282 | C/G | — | uncertain significance |
| rs577360735 | 16:86,588,345 | T/C | — | uncertain significance |
| rs760671587 | 16:86,588,351 | A/G | — | uncertain significance |
| rs2507915238 | 16:86,588,354 | C/G | — | uncertain significance |
| rs371051448 | 16:86,588,778 | C/T | — | uncertain significance |
| rs146689733 | 16:86,589,935 | G/A | upstream gene variant | — |
| rs140331433 | 16:86,590,187 | C/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.