GNL3
G protein nucleolar 3
Summary
The protein encoded by this gene may interact with p53 and may be involved in tumorigenesis. The encoded protein also appears to be important for stem cell proliferation. This protein is found in both the nucleus and nucleolus. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10865973 | 3:52,718,154 | A/G | — | — |
| rs10865974 | 3:52,718,280 | G/T | upstream gene variant | — |
| rs1108842 | 3:52,720,080 | A/G | — | — |
| rs368025635 | 3:52,720,119 | C/T | — | uncertain significance |
| rs11177 | 3:52,721,305 | G/A | missense variant | — |
| rs375460127 | 3:52,721,365 | C/T | — | uncertain significance |
| rs775062446 | 3:52,722,162 | C/T | — | uncertain significance |
| rs1561254155 | 3:52,723,184 | G/A | — | uncertain significance |
| rs142349859 | 3:52,723,208 | T/A | — | uncertain significance |
| rs188045558 | 3:52,723,835 | A/G | downstream gene variant | — |
| rs187015844 | 3:52,724,193 | G/A | downstream gene variant | — |
| rs369417968 | 3:52,724,962 | G/A | — | likely benign |
| rs372442220 | 3:52,724,983 | C/T | — | uncertain significance |
| rs375232066 | 3:52,724,988 | C/T | — | uncertain significance |
| rs147656173 | 3:52,725,000 | G/A | — | uncertain significance |
| rs780344228 | 3:52,725,033 | C/T | — | uncertain significance |
| rs2097327288 | 3:52,725,573 | G/A | — | uncertain significance |
| rs185526521 | 3:52,726,613 | G/A | downstream gene variant | — |
| rs971100528 | 3:52,726,947 | T/A | — | uncertain significance |
| rs746795082 | 3:52,726,949 | G/A | — | uncertain significance |
| rs1453940306 | 3:52,727,016 | C/T | — | uncertain significance |
| rs112181554 | 3:52,727,036 | A/C | — | uncertain significance |
| rs2289247 | 3:52,727,257 | G/C | — | likely benign |
| rs1313332026 | 3:52,727,452 | C/T | — | uncertain significance |
| rs199790197 | 3:52,727,504 | T/A | — | uncertain significance |
| rs2097329415 | 3:52,727,526 | A/C | — | uncertain significance |
| rs34216132 | 3:52,727,675 | G/C | missense variant | — |
| rs372615484 | 3:52,727,695 | G/A | — | uncertain significance |
| rs780896442 | 3:52,727,821 | G/A | — | uncertain significance |
| rs151237641 | 3:52,728,058 | C/G | — | likely benign |
| rs2552110968 | 3:52,728,102 | C/G | — | uncertain significance |
| rs140993833 | 3:52,728,225 | G/C | — | uncertain significance |
| rs2097330527 | 3:52,728,283 | T/G | — | uncertain significance |
| rs6976 | 3:52,728,804 | C/T | regulatory region variant | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.