METTL15
methyltransferase 15, mitochondrial 12S rRNA N4-cytidine
Summary
Enables rRNA (cytosine-N4-)-methyltransferase activity. Involved in rRNA base methylation. Is active in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs757256132 | 11:28,134,888 | C/T | — | uncertain significance |
| rs754479321 | 11:28,134,939 | G/A | — | uncertain significance |
| rs953667667 | 11:28,134,969 | C/G | — | uncertain significance |
| rs374210103 | 11:28,135,000 | A/G | — | uncertain significance |
| rs530544431 | 11:28,135,017 | C/T | — | uncertain significance |
| rs775566813 | 11:28,135,066 | A/G | — | uncertain significance |
| rs772086928 | 11:28,135,078 | A/G | — | uncertain significance |
| rs577282708 | 11:28,232,654 | A/G | — | uncertain significance |
| rs139932606 | 11:28,232,741 | T/C | — | uncertain significance |
| rs11601602 | 11:28,233,768 | A/G | intron variant | — |
| rs140429583 | 11:28,311,769 | A/G | — | likely benign |
| rs1856457368 | 11:28,311,796 | G/A | — | uncertain significance |
| rs773366749 | 11:28,311,839 | G/T | — | uncertain significance |
| rs746490910 | 11:28,311,883 | C/G | — | uncertain significance |
| rs545673517 | 11:28,313,905 | T/C | — | — |
| rs145619211 | 11:28,318,319 | G/A | — | uncertain significance |
| rs145080229 | 11:28,318,379 | G/A | — | uncertain significance |
| rs774073280 | 11:28,318,452 | C/T | — | uncertain significance |
| rs1420666931 | 11:28,351,967 | A/T | — | uncertain significance |
| rs369114838 | 11:28,351,972 | C/T | — | uncertain significance |
| rs760001083 | 11:28,351,973 | G/T | — | uncertain significance |
| rs1170095535 | 11:28,352,030 | G/A | — | uncertain significance |
| rs559762203 | 11:28,352,034 | A/G | — | uncertain significance |
| rs1849781827 | 11:28,352,072 | T/C | — | uncertain significance |
| rs377363969 | 11:28,352,101 | G/C | — | uncertain significance |
| rs371016812 | 11:28,352,108 | G/A | — | uncertain significance |
| rs1241374062 | 11:28,352,234 | G/A | — | likely benign |
| rs540205919 | 11:28,352,308 | G/A | — | uncertain significance |
| rs558701916 | 11:28,352,330 | A/T | — | uncertain significance |
| rs566042076 | 11:28,352,353 | C/T | — | uncertain significance |
| rs11030295 | 11:28,382,374 | G/C | — | — |
| rs12360793 | 11:28,384,757 | A/G | intron variant | — |
| rs12788184 | 11:28,389,866 | A/T | — | — |
| rs7129440 | 11:28,398,114 | G/A | intron variant | — |
| rs11030306 | 11:28,398,635 | C/T | — | — |
| rs11493473 | 11:28,412,843 | G/A | — | — |
| rs11030330 | 11:28,448,117 | C/T | intron variant | — |
| rs4923541 | 11:28,479,535 | C/T | intron variant | — |
| rs4923542 | 11:28,507,389 | T/G | intron variant | — |
| rs4359193 | 11:28,527,705 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.