GBP2
guanylate binding protein 2
Summary
This gene belongs to the guanine-binding protein (GBP) family, which includes interferon-induced proteins that can bind to guanine nucleotides (GMP, GDP and GTP). The encoded protein is a GTPase which hydrolyzes GTP, predominantly to GDP. The protein may play a role as a marker of squamous cell carcinomas. [provided by RefSeq, Jul 2013]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1681091768 | 1:89,573,878 | G/A | — | uncertain significance |
| rs766975415 | 1:89,573,908 | C/T | — | uncertain significance |
| rs1035972357 | 1:89,575,889 | G/T | — | uncertain significance |
| rs200764009 | 1:89,575,934 | T/G | — | uncertain significance |
| rs139664617 | 1:89,578,222 | C/T | — | uncertain significance |
| rs761974512 | 1:89,578,240 | G/A | — | uncertain significance |
| rs112956911 | 1:89,579,024 | C/A | intron variant | — |
| rs753229736 | 1:89,579,685 | A/G | — | likely risk allele |
| rs750141433 | 1:89,579,707 | T/C | — | likely benign |
| rs1240387966 | 1:89,579,749 | T/C | — | uncertain significance |
| rs754738734 | 1:89,579,848 | C/T | — | uncertain significance |
| rs749600192 | 1:89,579,875 | C/T | — | uncertain significance |
| rs540569552 | 1:89,581,095 | T/C | — | — |
| rs2523587861 | 1:89,582,698 | C/T | — | uncertain significance |
| rs745314942 | 1:89,582,822 | G/C | — | uncertain significance |
| rs143042903 | 1:89,582,825 | C/T | — | uncertain significance |
| rs369681409 | 1:89,582,881 | C/T | — | uncertain significance |
| rs754430142 | 1:89,583,392 | C/T | — | uncertain significance |
| rs1391203343 | 1:89,583,400 | G/A | — | uncertain significance |
| rs140765409 | 1:89,583,433 | C/T | — | uncertain significance |
| rs6428503 | 1:89,584,069 | T/C | intron variant | — |
| rs778125002 | 1:89,585,911 | C/T | — | uncertain significance |
| rs1347801425 | 1:89,585,932 | T/G | — | uncertain significance |
| rs386352304 | 1:89,585,969 | A/C | — | uncertain significance |
| rs147250118 | 1:89,586,829 | C/T | — | likely benign |
| rs201393649 | 1:89,586,833 | A/C | — | uncertain significance |
| rs375271390 | 1:89,586,855 | C/T | — | uncertain significance |
| rs756471807 | 1:89,586,893 | G/T | — | uncertain significance |
| rs1265107317 | 1:89,587,495 | G/C | — | uncertain significance |
| rs745556196 | 1:89,587,507 | C/A | — | uncertain significance |
| rs775100378 | 1:89,587,508 | G/A | — | uncertain significance |
| rs140687152 | 1:89,587,545 | C/T | — | likely benign |
| rs149938333 | 1:89,587,575 | T/C | — | likely benign |
| rs2523600454 | 1:89,587,628 | G/A | — | uncertain significance |
| rs10922573 | 1:89,588,380 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.