GNB4
G protein subunit beta 4
Summary
Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. [provided by RefSeq, Jul 2008]
Known Variants224 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3774225 | 3:179,118,998 | C/T | — | benign |
| rs2473872576 | 3:179,119,004 | A/G | — | likely benign |
| rs2108575061 | 3:179,119,043 | C/T | — | likely benign |
| rs61750380 | 3:179,119,066 | C/A | — | uncertain significance |
| rs1404664675 | 3:179,119,067 | A/C | — | likely benign |
| rs1324179212 | 3:179,119,072 | A/G | — | likely benign |
| rs747095396 | 3:179,119,083 | C/T | — | uncertain significance |
| rs769787081 | 3:179,119,097 | A/T | — | likely benign |
| rs1168008697 | 3:179,119,101 | A/G | — | uncertain significance |
| rs879100241 | 3:179,119,103 | G/A | — | likely benign |
| rs1351274064 | 3:179,119,105 | C/A | — | uncertain significance |
| rs1714292732 | 3:179,119,106 | A/C | — | conflicting classifications of pathogenicity |
| rs938943088 | 3:179,119,112 | A/G | — | uncertain significance |
| rs749107679 | 3:179,119,117 | A/G | — | likely benign |
| rs2108575181 | 3:179,119,122 | C/A | — | likely benign |
| rs370399077 | 3:179,119,126 | A/G | — | likely benign |
| rs1261447203 | 3:179,119,127 | A/G | — | likely benign |
| rs186397073 | 3:179,119,136 | C/T | — | likely benign |
| rs78652099 | 3:179,119,300 | G/A | — | benign |
| rs28642912 | 3:179,119,373 | C/T | — | benign |
| rs6792342 | 3:179,119,399 | A/G | — | benign |
| rs2287311 | 3:179,122,707 | C/G | — | benign |
| rs2287310 | 3:179,122,918 | C/T | — | benign |
| rs777723439 | 3:179,122,958 | A/C | — | likely benign |
| rs1714426501 | 3:179,122,961 | T/G | — | likely benign |
| rs749160674 | 3:179,122,962 | G/C | — | likely benign |
| rs371633908 | 3:179,122,968 | A/G | — | likely benign |
| rs376068792 | 3:179,122,969 | T/C | — | likely benign |
| rs2108579668 | 3:179,122,975 | A/G | — | uncertain significance |
| rs1281047589 | 3:179,122,979 | T/C | — | uncertain significance |
| rs771664047 | 3:179,122,983 | C/T | — | uncertain significance |
| rs201776673 | 3:179,122,984 | G/A | — | uncertain significance |
| rs1020090528 | 3:179,122,986 | T/G | — | uncertain significance |
| rs1167931862 | 3:179,122,991 | T/A | — | uncertain significance |
| rs1390536220 | 3:179,122,996 | G/C | — | uncertain significance |
| rs1431464178 | 3:179,122,997 | C/T | — | likely benign |
| rs202181846 | 3:179,122,998 | G/A | — | likely benign |
| rs550870195 | 3:179,123,009 | A/G | — | likely benign |
| rs1398073875 | 3:179,123,027 | G/A | — | likely benign |
| rs2473881961 | 3:179,123,031 | C/G | — | uncertain significance |
| rs554623238 | 3:179,123,041 | A/C | — | likely benign |
| rs186593898 | 3:179,123,046 | C/G | — | uncertain significance |
| rs1714430172 | 3:179,123,047 | G/A | — | uncertain significance |
| rs1367787021 | 3:179,123,055 | T/C | — | uncertain significance |
| rs540700486 | 3:179,123,060 | G/T | — | uncertain significance |
| rs139774004 | 3:179,123,068 | C/T | — | uncertain significance |
| rs2473882155 | 3:179,123,070 | G/A | — | uncertain significance |
| rs200411099 | 3:179,123,091 | T/C | — | conflicting classifications of pathogenicity |
| rs2108579874 | 3:179,123,094 | T/C | — | uncertain significance |
| rs752762550 | 3:179,123,095 | C/T | — | uncertain significance |
| rs375559586 | 3:179,123,097 | T/C | — | uncertain significance |
| rs1560209707 | 3:179,123,105 | C/T | — | likely benign |
| rs778880529 | 3:179,123,107 | A/G | — | likely benign |
| rs1714433223 | 3:179,123,110 | A/G | — | likely benign |
| rs1376881475 | 3:179,123,111 | T/C | — | likely benign |
| rs878855069 | 3:179,123,123 | T/C | — | likely benign |
| rs971032854 | 3:179,123,128 | G/A | — | uncertain significance |
| rs368061934 | 3:179,123,135 | A/C | — | uncertain significance |
| rs371587505 | 3:179,123,138 | G/C | — | likely benign |
| rs770241406 | 3:179,123,142 | C/T | — | uncertain significance |
| rs756270613 | 3:179,123,143 | G/A | — | uncertain significance |
| rs763262757 | 3:179,123,144 | G/A | — | likely benign |
| rs2108580038 | 3:179,123,145 | C/T | — | uncertain significance |
| rs774571998 | 3:179,123,147 | A/C | — | likely benign |
| rs2473882548 | 3:179,123,149 | T/G | — | uncertain significance |
| rs1207477015 | 3:179,123,150 | G/A | — | likely benign |
| rs1714435843 | 3:179,123,161 | A/T | — | uncertain significance |
| rs751400013 | 3:179,123,170 | C/T | — | conflicting classifications of pathogenicity |
| rs752815541 | 3:179,123,171 | G/A | — | likely benign |
| rs1433615086 | 3:179,123,180 | T/C | — | likely benign |
| rs758131126 | 3:179,123,185 | T/G | — | conflicting classifications of pathogenicity |
| rs199620294 | 3:179,123,197 | A/G | — | uncertain significance |
| rs751385040 | 3:179,123,200 | C/T | — | likely benign |
| rs2108580139 | 3:179,123,203 | G/C | — | uncertain significance |
| rs2108580143 | 3:179,123,204 | A/C | — | likely benign |
| rs780957835 | 3:179,123,212 | A/C | — | likely benign |
| rs76492501 | 3:179,123,429 | A/G | — | likely benign |
| rs186562247 | 3:179,130,913 | C/T | — | likely benign |
| rs116068524 | 3:179,131,063 | T/C | — | likely benign |
| rs2108589120 | 3:179,131,186 | T/C | — | likely benign |
| rs1016827159 | 3:179,131,188 | C/T | — | likely benign |
| rs1433602623 | 3:179,131,190 | A/G | — | likely benign |
| rs1422199544 | 3:179,131,201 | C/G | — | uncertain significance |
| rs538233963 | 3:179,131,202 | T/C | — | likely benign |
| rs1459911526 | 3:179,131,210 | T/C | — | uncertain significance |
| rs2108589151 | 3:179,131,218 | T/C | — | likely benign |
| rs751438259 | 3:179,131,230 | C/T | — | likely benign |
| rs144385061 | 3:179,131,231 | G/A | — | likely benign |
| rs199615251 | 3:179,131,240 | T/C | — | likely pathogenic |
| rs755596977 | 3:179,131,254 | A/C | — | uncertain significance |
| rs2473900718 | 3:179,131,258 | C/T | — | uncertain significance |
| rs748747265 | 3:179,131,259 | G/A | — | uncertain significance |
| rs1341252890 | 3:179,131,263 | A/G | — | likely benign |
| rs779372670 | 3:179,131,269 | T/A | — | uncertain significance |
| rs2473900767 | 3:179,131,275 | G/A | — | likely benign |
| rs775578986 | 3:179,131,301 | C/T | — | conflicting classifications of pathogenicity |
| rs760894139 | 3:179,131,303 | A/T | — | uncertain significance |
| rs768745441 | 3:179,131,305 | A/G | — | likely benign |
| rs776836938 | 3:179,131,307 | T/A | — | conflicting classifications of pathogenicity |
| rs2473900887 | 3:179,131,315 | T/C | — | uncertain significance |
Showing 100 of 224 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.