EFR3B
EFR3 homolog B
Summary
Involved in phosphatidylinositol phosphate biosynthetic process and protein localization to plasma membrane. Located in actin cytoskeleton; cytosol; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6733301 | 2:25,276,284 | G/T | — | — |
| rs1971136 | 2:25,291,539 | C/G | — | — |
| rs2384078 | 2:25,294,418 | G/T | — | — |
| rs478222 | 2:25,301,755 | A/T | regulatory region variant | — |
| rs1530016 | 2:25,305,756 | C/T | upstream gene variant | — |
| rs564667 | 2:25,310,860 | A/T | intron variant | — |
| rs370067502 | 2:25,315,912 | A/G | — | uncertain significance |
| rs772911555 | 2:25,315,950 | G/A | — | uncertain significance |
| rs371551570 | 2:25,315,964 | G/C | — | uncertain significance |
| rs1157170656 | 2:25,315,974 | C/T | — | uncertain significance |
| rs2438679 | 2:25,317,653 | C/G | — | — |
| rs519111 | 2:25,333,735 | T/C | intron variant | — |
| rs1313668199 | 2:25,344,563 | G/A | — | uncertain significance |
| rs765652835 | 2:25,344,633 | C/T | — | uncertain significance |
| rs1273096169 | 2:25,344,660 | C/A | — | uncertain significance |
| rs996433592 | 2:25,352,977 | A/G | — | uncertain significance |
| rs1030409089 | 2:25,353,431 | A/T | — | uncertain significance |
| rs753414525 | 2:25,354,258 | A/C | — | uncertain significance |
| rs1446665291 | 2:25,354,690 | G/T | — | uncertain significance |
| rs1404661120 | 2:25,354,723 | A/G | — | uncertain significance |
| rs553917604 | 2:25,355,861 | G/A | — | uncertain significance |
| rs1215126518 | 2:25,355,882 | G/A | — | uncertain significance |
| rs2465478237 | 2:25,358,469 | T/C | — | uncertain significance |
| rs1413477557 | 2:25,359,450 | A/G | — | uncertain significance |
| rs201336240 | 2:25,359,453 | G/A | — | uncertain significance |
| rs902324075 | 2:25,360,226 | A/G | — | uncertain significance |
| rs1482195002 | 2:25,360,283 | C/T | — | uncertain significance |
| rs368601264 | 2:25,360,351 | C/T | — | uncertain significance |
| rs770082853 | 2:25,360,357 | G/C | — | uncertain significance |
| rs2465482982 | 2:25,360,364 | C/T | — | uncertain significance |
| rs1436978448 | 2:25,361,930 | C/A | — | uncertain significance |
| rs2465487573 | 2:25,362,057 | G/A | — | uncertain significance |
| rs4665766 | 2:25,366,130 | A/C | — | — |
| rs369688644 | 2:25,366,667 | A/T | — | uncertain significance |
| rs894718994 | 2:25,367,837 | C/T | — | uncertain significance |
| rs199969836 | 2:25,367,838 | G/A | — | uncertain significance |
| rs79274160 | 2:25,368,951 | G/T | — | — |
| rs1561288 | 2:25,369,002 | C/T | intron variant | — |
| rs777702211 | 2:25,372,564 | G/A | — | uncertain significance |
| rs13401333 | 2:25,373,031 | C/G | — | — |
| rs13428823 | 2:25,373,298 | G/A | intron variant | — |
| rs1490096329 | 2:25,374,783 | T/G | — | uncertain significance |
| rs1002111822 | 2:25,374,791 | G/A | — | uncertain significance |
| rs1318768200 | 2:25,374,818 | C/T | — | uncertain significance |
| rs749285945 | 2:25,374,875 | C/T | — | uncertain significance |
| rs1013343231 | 2:25,374,888 | G/A | — | uncertain significance |
| rs549836377 | 2:25,377,136 | C/T | — | uncertain significance |
| rs1262329645 | 2:25,377,192 | G/A | — | uncertain significance |
| rs2118404 | 2:25,377,329 | C/A | — | — |
| rs7589318 | 2:25,378,372 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.