CAMKMT
calmodulin-lysine N-methyltransferase
Summary
This gene encodes a class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin. The protein contains a AdoMet-binding motif and may play a role in calcium-dependent signaling. [provided by RefSeq, Sep 2012]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2466524942 | 2:44,589,165 | G/C | — | uncertain significance |
| rs750780281 | 2:44,589,175 | C/T | — | uncertain significance |
| rs756670915 | 2:44,589,177 | G/A | — | uncertain significance |
| rs989336819 | 2:44,589,192 | G/A | — | uncertain significance |
| rs894734482 | 2:44,589,240 | G/A | — | uncertain significance |
| rs2466525935 | 2:44,589,250 | C/G | — | uncertain significance |
| rs777078703 | 2:44,589,264 | C/G | — | uncertain significance |
| rs945626575 | 2:44,599,892 | A/T | — | uncertain significance |
| rs200227404 | 2:44,617,382 | A/G | — | uncertain significance |
| rs757346624 | 2:44,617,384 | A/C | — | uncertain significance |
| rs374314875 | 2:44,617,411 | G/T | — | uncertain significance |
| rs1067327 | 2:44,628,529 | C/A | — | — |
| rs1067361 | 2:44,661,217 | G/A | — | — |
| rs13414205 | 2:44,662,475 | C/T | intron variant | — |
| rs556971810 | 2:44,663,206 | T/A | — | — |
| rs140879085 | 2:44,663,302 | C/T | intron variant | — |
| rs10190127 | 2:44,694,382 | A/C | intron variant | — |
| rs698813 | 2:44,705,615 | A/G | intron variant | — |
| rs72881110 | 2:44,754,020 | T/A | intron variant | — |
| rs11124991 | 2:44,764,879 | T/G | — | — |
| rs2341459 | 2:44,768,202 | T/C | intron variant | — |
| rs2880052 | 2:44,768,265 | G/A | intron variant | — |
| rs56205860 | 2:44,770,731 | G/T | intron variant | — |
| rs7578811 | 2:44,834,956 | T/G | intron variant | — |
| rs6744794 | 2:44,842,145 | C/T | — | — |
| rs61326631 | 2:44,848,524 | T/A | — | — |
| rs12468040 | 2:44,854,981 | T/G | intron variant | — |
| rs1579641 | 2:44,862,139 | G/C | — | — |
| rs4324362 | 2:44,866,893 | G/T | — | — |
| rs72792395 | 2:44,886,144 | C/T | intron variant | — |
| rs2465936838 | 2:44,931,430 | C/T | — | uncertain significance |
| rs371521737 | 2:44,933,475 | C/T | — | uncertain significance |
| rs1030035618 | 2:44,934,559 | A/G | — | uncertain significance |
| rs2465984238 | 2:44,942,428 | G/T | — | uncertain significance |
| rs760155636 | 2:44,942,433 | A/T | — | uncertain significance |
| rs542723780 | 2:44,942,444 | C/T | — | uncertain significance |
| rs779962351 | 2:44,942,464 | G/A | — | uncertain significance |
| rs747046842 | 2:44,970,769 | G/A | — | uncertain significance |
| rs1679798735 | 2:44,970,786 | G/T | — | uncertain significance |
| rs1350210346 | 2:44,970,787 | A/G | — | uncertain significance |
| rs343949 | 2:44,973,791 | A/G | — | — |
| rs759251420 | 2:44,981,219 | A/G | — | uncertain significance |
| rs201420188 | 2:44,993,577 | G/A | — | likely benign |
| rs1330795382 | 2:44,993,603 | A/G | — | uncertain significance |
| rs754054502 | 2:44,993,605 | A/G | — | uncertain significance |
| rs150667583 | 2:44,993,652 | C/T | — | benign |
| rs200454460 | 2:44,999,192 | G/A | — | likely benign |
| rs549234222 | 2:44,999,198 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.