SMYD3
SET and MYND domain containing 3
Summary
This gene encodes a histone methyltransferase which functions in RNA polymerase II complexes by an interaction with a specific RNA helicase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs994995027 | 1:245,927,363 | C/T | — | uncertain significance |
| rs12065652 | 1:246,078,824 | C/T | — | benign |
| rs533568761 | 1:246,078,836 | T/C | — | uncertain significance |
| rs952048801 | 1:246,078,854 | A/C | — | uncertain significance |
| rs987211168 | 1:246,078,896 | C/T | — | uncertain significance |
| rs781096043 | 1:246,078,899 | C/T | — | uncertain significance |
| rs2527649195 | 1:246,078,930 | A/G | — | uncertain significance |
| rs143716511 | 1:246,078,936 | T/A | — | uncertain significance |
| rs147009044 | 1:246,091,247 | C/T | — | uncertain significance |
| rs549272016 | 1:246,091,255 | C/T | — | uncertain significance |
| rs755914433 | 1:246,091,264 | C/T | — | uncertain significance |
| rs1214851067 | 1:246,091,285 | T/C | — | uncertain significance |
| rs1054051754 | 1:246,093,199 | T/C | — | uncertain significance |
| rs12117603 | 1:246,155,107 | T/G | intron variant | — |
| rs28468565 | 1:246,157,144 | G/T | — | — |
| rs6693295 | 1:246,223,120 | C/T | intron variant | — |
| rs2788015 | 1:246,242,908 | C/A | — | — |
| rs10802346 | 1:246,372,880 | G/A | — | — |
| rs140841346 | 1:246,376,220 | C/G | regulatory region variant | — |
| rs115269913 | 1:246,391,431 | C/T | intron variant | — |
| rs552900551 | 1:246,392,900 | T/C | — | — |
| rs150866915 | 1:246,405,568 | G/T | intron variant | — |
| rs144514515 | 1:246,490,571 | T/C | — | uncertain significance |
| rs756702699 | 1:246,490,592 | C/T | — | uncertain significance |
| rs747083559 | 1:246,490,618 | T/G | — | uncertain significance |
| rs770911084 | 1:246,490,639 | T/C | — | uncertain significance |
| rs1276776803 | 1:246,493,794 | C/A | — | uncertain significance |
| rs143920876 | 1:246,498,697 | C/T | — | uncertain significance |
| rs752754685 | 1:246,498,707 | C/G | — | uncertain significance |
| rs999674703 | 1:246,498,724 | T/G | — | uncertain significance |
| rs148874023 | 1:246,498,730 | C/A | — | uncertain significance |
| rs992809841 | 1:246,498,754 | T/C | — | uncertain significance |
| rs11544849 | 1:246,518,360 | G/A | — | benign |
| rs769227482 | 1:246,518,364 | C/T | — | uncertain significance |
| rs138004389 | 1:246,518,365 | G/A | — | uncertain significance |
| rs1368723920 | 1:246,539,747 | G/C | — | — |
| rs532166355 | 1:246,658,479 | A/G | — | — |
| rs11800820 | 1:246,661,236 | C/A | — | — |
| rs755429858 | 1:246,670,461 | G/A | — | uncertain significance |
| rs2068557962 | 1:246,670,464 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.