GAB4
GRB2 associated binding protein family member 4
Summary
Predicted to enable transmembrane receptor protein tyrosine kinase adaptor activity. Predicted to be involved in signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs754860854 | 22:17,443,699 | T/A | — | uncertain significance |
| rs770624257 | 22:17,443,739 | T/C | — | likely benign |
| rs748653350 | 22:17,444,659 | T/G | — | uncertain significance |
| rs199551459 | 22:17,444,667 | G/C | — | uncertain significance |
| rs200669352 | 22:17,444,715 | G/A | — | uncertain significance |
| rs2517335962 | 22:17,445,695 | G/C | — | uncertain significance |
| rs760414737 | 22:17,447,113 | A/C | — | likely benign |
| rs757955159 | 22:17,447,126 | G/C | — | uncertain significance |
| rs375901031 | 22:17,447,137 | C/G | — | uncertain significance |
| rs761671659 | 22:17,447,167 | C/A | — | uncertain significance |
| rs201893836 | 22:17,447,169 | G/A | — | likely benign |
| rs200930866 | 22:17,447,184 | C/G | — | uncertain significance |
| rs200334935 | 22:17,449,273 | G/A | — | uncertain significance |
| rs182948629 | 22:17,450,461 | C/T | intron variant | — |
| rs920440970 | 22:17,450,839 | T/A | — | uncertain significance |
| rs201405868 | 22:17,450,841 | T/A | — | uncertain significance |
| rs370292871 | 22:17,450,844 | G/A | — | uncertain significance |
| rs373491367 | 22:17,450,860 | G/A | — | uncertain significance |
| rs377466804 | 22:17,450,863 | T/C | — | uncertain significance |
| rs1488721206 | 22:17,450,877 | C/T | — | uncertain significance |
| rs202215160 | 22:17,450,898 | G/A | — | uncertain significance |
| rs200505777 | 22:17,450,899 | G/A | — | uncertain significance |
| rs368140874 | 22:17,450,904 | C/A | — | uncertain significance |
| rs2517353095 | 22:17,450,935 | G/A | — | uncertain significance |
| rs367789494 | 22:17,450,946 | T/C | — | uncertain significance |
| rs1243714209 | 22:17,450,962 | A/C | — | uncertain significance |
| rs372130793 | 22:17,450,971 | T/G | — | uncertain significance |
| rs1311563327 | 22:17,450,995 | T/C | — | uncertain significance |
| rs369396073 | 22:17,451,046 | T/A | — | uncertain significance |
| rs200236379 | 22:17,468,875 | C/T | — | uncertain significance |
| rs199813045 | 22:17,468,893 | G/A | — | uncertain significance |
| rs201740103 | 22:17,468,901 | G/A | — | uncertain significance |
| rs1241385922 | 22:17,468,904 | G/A | — | uncertain significance |
| rs560437811 | 22:17,468,907 | G/A | — | uncertain significance |
| rs200048737 | 22:17,468,928 | G/A | — | uncertain significance |
| rs377709316 | 22:17,472,792 | A/T | — | uncertain significance |
| rs765692227 | 22:17,472,819 | T/G | — | uncertain significance |
| rs912853748 | 22:17,472,870 | T/C | — | uncertain significance |
| rs2517403810 | 22:17,473,023 | C/T | — | uncertain significance |
| rs2517429595 | 22:17,488,833 | A/G | — | uncertain significance |
| rs774854537 | 22:17,488,857 | G/T | — | uncertain significance |
| rs1464842908 | 22:17,488,874 | C/T | — | uncertain significance |
| rs1408450899 | 22:17,488,957 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.