PRDM7
PR/SET domain 7
Summary
This gene encodes a member of a family of proteins that may have roles in transcription and other nuclear processes. The encoded protein contains a KRAB (Kruppel-associated box) domain -A box and a SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain and may function as a histone methyltransferase. [provided by RefSeq, Aug 2013]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2543545092 | 16:90,126,814 | T/G | — | uncertain significance |
| rs201936074 | 16:90,126,859 | C/T | — | uncertain significance |
| rs765704768 | 16:90,126,870 | A/G | — | uncertain significance |
| rs756844091 | 16:90,126,909 | C/A | — | uncertain significance |
| rs774946141 | 16:90,126,952 | A/G | — | uncertain significance |
| rs750230701 | 16:90,126,970 | G/C | — | uncertain significance |
| rs200324057 | 16:90,126,998 | C/G | — | uncertain significance |
| rs771360070 | 16:90,127,012 | C/G | — | uncertain significance |
| rs201215666 | 16:90,127,014 | C/T | — | uncertain significance |
| rs2037759528 | 16:90,127,017 | G/T | — | uncertain significance |
| rs147880743 | 16:90,127,903 | C/T | — | uncertain significance |
| rs748279339 | 16:90,128,384 | T/C | — | uncertain significance |
| rs148866266 | 16:90,128,424 | C/T | — | uncertain significance |
| rs766560166 | 16:90,128,428 | C/G | — | uncertain significance |
| rs778516297 | 16:90,128,456 | C/T | — | uncertain significance |
| rs925888818 | 16:90,128,478 | C/T | — | uncertain significance |
| rs2543550331 | 16:90,128,824 | C/A | — | uncertain significance |
| rs188033705 | 16:90,128,876 | A/G | — | likely benign |
| rs372056005 | 16:90,130,121 | G/A | — | uncertain significance |
| rs928245877 | 16:90,130,154 | T/C | — | likely benign |
| rs765132852 | 16:90,130,160 | G/A | — | uncertain significance |
| rs766235686 | 16:90,133,280 | T/C | — | uncertain significance |
| rs550845267 | 16:90,133,782 | C/G | — | — |
| rs534223674 | 16:90,134,084 | T/A | — | — |
| rs773645588 | 16:90,141,779 | T/C | — | uncertain significance |
| rs536731786 | 16:90,141,803 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.