METTL25B
methyltransferase like 25B
Summary
Predicted to enable rRNA (adenine-N6,N6-)-dimethyltransferase activity. Predicted to be involved in rRNA methylation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200685743 | 1:156,698,943 | A/G | — | uncertain significance |
| rs139389257 | 1:156,698,979 | A/G | — | uncertain significance |
| rs12145743 | 1:156,700,651 | T/G | upstream gene variant | — |
| rs145008223 | 1:156,701,804 | T/C | — | uncertain significance |
| rs755014168 | 1:156,701,807 | G/C | — | uncertain significance |
| rs368662106 | 1:156,702,198 | G/A | — | uncertain significance |
| rs756510806 | 1:156,702,215 | C/T | — | uncertain significance |
| rs118116867 | 1:156,702,216 | G/A | — | uncertain significance |
| rs754203979 | 1:156,702,218 | A/G | — | uncertain significance |
| rs889275667 | 1:156,702,796 | A/G | — | uncertain significance |
| rs367820508 | 1:156,702,825 | G/A | — | uncertain significance |
| rs146477892 | 1:156,703,207 | G/T | — | uncertain significance |
| rs2525053145 | 1:156,703,244 | G/A | — | uncertain significance |
| rs569829775 | 1:156,703,820 | G/A | — | uncertain significance |
| rs146818149 | 1:156,703,837 | G/A | — | uncertain significance |
| rs201514643 | 1:156,703,854 | C/A | — | uncertain significance |
| rs2525060455 | 1:156,703,880 | T/C | — | uncertain significance |
| rs369102767 | 1:156,703,915 | C/G | — | uncertain significance |
| rs141153654 | 1:156,703,916 | G/A | — | uncertain significance |
| rs1649521928 | 1:156,703,931 | G/A | — | uncertain significance |
| rs889209689 | 1:156,703,948 | G/A | — | uncertain significance |
| rs374051320 | 1:156,703,961 | C/G | — | uncertain significance |
| rs761953821 | 1:156,704,086 | T/C | — | uncertain significance |
| rs777598412 | 1:156,704,108 | G/A | — | uncertain significance |
| rs772047048 | 1:156,704,128 | C/G | — | uncertain significance |
| rs373474927 | 1:156,704,181 | C/G | — | uncertain significance |
| rs531073742 | 1:156,704,188 | C/G | — | uncertain significance |
| rs776471319 | 1:156,704,215 | C/T | — | uncertain significance |
| rs759685694 | 1:156,704,222 | G/A | — | likely benign |
| rs754255191 | 1:156,704,236 | C/G | — | uncertain significance |
| rs768650526 | 1:156,704,258 | C/A | — | uncertain significance |
| rs61813557 | 1:156,704,613 | G/A | downstream gene variant | — |
| rs1456003100 | 1:156,705,573 | T/C | — | uncertain significance |
| rs763330536 | 1:156,705,677 | C/T | — | uncertain significance |
| rs41267417 | 1:156,706,024 | C/T | downstream gene variant | — |
| rs372196050 | 1:156,706,438 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.