NUGGC
nuclear GTPase, germinal center associated
Summary
Enables GTPase activity. Involved in cellular response to lipopolysaccharide; negative regulation of apoptotic process; and regulation of nuclear cell cycle DNA replication. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs376263360 | 8:27,880,848 | C/T | — | uncertain significance |
| rs750907742 | 8:27,880,850 | G/A | — | uncertain significance |
| rs201330243 | 8:27,880,854 | G/T | — | uncertain significance |
| rs369859443 | 8:27,880,871 | G/C | — | uncertain significance |
| rs549505578 | 8:27,880,911 | G/A | — | uncertain significance |
| rs751556152 | 8:27,880,944 | G/T | — | uncertain significance |
| rs1563210939 | 8:27,880,976 | A/G | — | uncertain significance |
| rs369064910 | 8:27,884,560 | C/T | — | uncertain significance |
| rs377099582 | 8:27,886,850 | C/T | — | uncertain significance |
| rs756785058 | 8:27,886,883 | C/T | — | uncertain significance |
| rs2486553944 | 8:27,886,887 | C/T | — | uncertain significance |
| rs2486554055 | 8:27,886,906 | G/C | — | uncertain significance |
| rs974664756 | 8:27,887,902 | T/C | — | uncertain significance |
| rs374100228 | 8:27,887,910 | T/C | — | uncertain significance |
| rs368713059 | 8:27,888,795 | A/G | — | uncertain significance |
| rs756794412 | 8:27,888,799 | C/A | — | uncertain significance |
| rs377427046 | 8:27,888,896 | G/A | — | uncertain significance |
| rs1809477841 | 8:27,891,088 | G/T | — | uncertain significance |
| rs1007194379 | 8:27,891,096 | A/G | — | uncertain significance |
| rs757286822 | 8:27,891,132 | G/A | — | uncertain significance |
| rs931945803 | 8:27,891,148 | C/T | — | uncertain significance |
| rs757000938 | 8:27,891,214 | T/C | — | uncertain significance |
| rs200817436 | 8:27,898,593 | C/T | — | uncertain significance |
| rs752260434 | 8:27,898,644 | C/T | — | uncertain significance |
| rs373371560 | 8:27,898,648 | C/T | — | uncertain significance |
| rs1176522817 | 8:27,898,704 | C/T | — | uncertain significance |
| rs202084810 | 8:27,903,083 | C/T | — | likely benign |
| rs2486587784 | 8:27,903,106 | C/T | — | uncertain significance |
| rs6983473 | 8:27,905,888 | A/G | — | — |
| rs563017713 | 8:27,918,013 | G/A | — | uncertain significance |
| rs559375149 | 8:27,922,053 | C/T | — | uncertain significance |
| rs377376383 | 8:27,922,073 | T/C | — | uncertain significance |
| rs201814798 | 8:27,922,110 | C/T | — | uncertain significance |
| rs1199948316 | 8:27,922,179 | C/T | — | uncertain significance |
| rs116792344 | 8:27,922,195 | A/G | — | likely benign |
| rs767520160 | 8:27,922,241 | T/C | — | uncertain significance |
| rs4732812 | 8:27,923,388 | C/T | intron variant | — |
| rs750709442 | 8:27,925,050 | A/T | — | uncertain significance |
| rs755083542 | 8:27,925,086 | G/A | — | uncertain significance |
| rs752851999 | 8:27,925,092 | A/C | — | uncertain significance |
| rs764541235 | 8:27,925,852 | T/C | — | uncertain significance |
| rs745359784 | 8:27,925,935 | A/G | — | uncertain significance |
| rs376712154 | 8:27,927,152 | G/A | — | uncertain significance |
| rs369590529 | 8:27,927,778 | G/C | — | uncertain significance |
| rs182991073 | 8:27,927,796 | A/G | — | uncertain significance |
| rs200051716 | 8:27,927,822 | C/T | — | uncertain significance |
| rs893767414 | 8:27,927,858 | T/C | — | uncertain significance |
| rs79485384 | 8:27,938,501 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.