FRMD4B
FERM domain containing 4B
Summary
This gene encodes a GRP1-binding protein which contains a FERM protein interaction domain as well as two coiled coil domains. This protein may play a role as a scaffolding protein. [provided by RefSeq, Mar 2014]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375814018 | 3:69,221,079 | T/A | — | uncertain significance |
| rs777039046 | 3:69,221,104 | C/G | — | uncertain significance |
| rs374013656 | 3:69,221,117 | G/C | — | uncertain significance |
| rs4473559 | 3:69,222,863 | T/G | intron variant | — |
| rs1485044270 | 3:69,225,759 | C/T | — | uncertain significance |
| rs6787362 | 3:69,227,379 | A/G | intron variant | — |
| rs4855360 | 3:69,229,725 | G/A | intron variant | — |
| rs199933053 | 3:69,230,070 | C/T | — | uncertain significance |
| rs768563202 | 3:69,230,127 | C/T | — | uncertain significance |
| rs540273782 | 3:69,230,154 | G/A | — | likely benign |
| rs769852415 | 3:69,230,169 | T/C | — | uncertain significance |
| rs192984298 | 3:69,230,224 | C/A | — | likely benign |
| rs777328436 | 3:69,230,298 | T/A | — | uncertain significance |
| rs1434179053 | 3:69,230,310 | C/T | — | uncertain significance |
| rs756184115 | 3:69,230,326 | C/T | — | uncertain significance |
| rs368398474 | 3:69,230,355 | C/T | — | uncertain significance |
| rs376166259 | 3:69,230,383 | G/A | — | uncertain significance |
| rs2471389879 | 3:69,230,431 | C/T | — | uncertain significance |
| rs372262060 | 3:69,230,459 | C/G | — | uncertain significance |
| rs61737529 | 3:69,230,511 | T/C | — | uncertain significance |
| rs200270906 | 3:69,230,554 | C/G | — | uncertain significance |
| rs200552074 | 3:69,230,605 | A/T | — | uncertain significance |
| rs764340324 | 3:69,230,613 | C/T | — | uncertain significance |
| rs200237674 | 3:69,230,622 | G/C | — | uncertain significance |
| rs532569537 | 3:69,230,637 | G/T | — | uncertain significance |
| rs202099937 | 3:69,230,847 | G/C | — | uncertain significance |
| rs201890981 | 3:69,231,791 | G/A | — | uncertain significance |
| rs781308604 | 3:69,231,800 | A/G | — | uncertain significance |
| rs748078460 | 3:69,231,819 | G/C | — | uncertain significance |
| rs377577151 | 3:69,231,822 | G/A | — | uncertain significance |
| rs760171258 | 3:69,231,864 | T/C | — | uncertain significance |
| rs371064682 | 3:69,236,958 | A/G | — | uncertain significance |
| rs191669150 | 3:69,236,999 | G/T | — | uncertain significance |
| rs780590235 | 3:69,237,002 | G/T | — | uncertain significance |
| rs2471492748 | 3:69,242,909 | T/C | — | uncertain significance |
| rs199520789 | 3:69,242,912 | C/T | — | uncertain significance |
| rs894108788 | 3:69,242,984 | T/C | — | uncertain significance |
| rs2092885927 | 3:69,244,216 | C/T | — | uncertain significance |
| rs1181651364 | 3:69,244,390 | G/A | — | uncertain significance |
| rs766669164 | 3:69,244,396 | A/C | — | uncertain significance |
| rs1365228214 | 3:69,244,400 | C/A | — | uncertain significance |
| rs200234607 | 3:69,244,405 | T/C | — | uncertain significance |
| rs76641825 | 3:69,244,732 | C/A | regulatory region variant | — |
| rs373596239 | 3:69,245,453 | G/A | — | uncertain significance |
| rs376190505 | 3:69,245,508 | T/C | — | uncertain significance |
| rs149242121 | 3:69,245,529 | T/C | — | uncertain significance |
| rs762220290 | 3:69,245,547 | C/A | — | uncertain significance |
| rs763965475 | 3:69,246,064 | C/T | — | uncertain significance |
| rs367935491 | 3:69,246,188 | T/G | — | uncertain significance |
| rs189397393 | 3:69,247,917 | T/C | — | likely benign |
| rs6806528 | 3:69,252,899 | C/T | regulatory region variant | — |
| rs201203228 | 3:69,265,418 | C/T | — | uncertain significance |
| rs202136321 | 3:69,265,419 | G/A | — | uncertain significance |
| rs2471643315 | 3:69,265,446 | A/G | — | uncertain significance |
| rs1288736463 | 3:69,265,447 | T/G | — | uncertain significance |
| rs2471643861 | 3:69,265,490 | C/T | — | uncertain significance |
| rs72932156 | 3:69,270,725 | C/G | intron variant | — |
| rs371721004 | 3:69,273,837 | C/T | — | uncertain significance |
| rs138895278 | 3:69,276,060 | G/T | intron variant | — |
| rs74633073 | 3:69,278,898 | C/A | — | — |
| rs765995914 | 3:69,298,380 | G/A | — | uncertain significance |
| rs35233461 | 3:69,325,524 | A/T | — | — |
| rs201892325 | 3:69,336,917 | C/T | — | uncertain significance |
| rs765555616 | 3:69,336,971 | T/C | — | uncertain significance |
| rs11128121 | 3:69,338,070 | C/G | — | — |
| rs1461818227 | 3:69,351,515 | G/A | — | uncertain significance |
| rs370199811 | 3:69,351,554 | C/T | — | uncertain significance |
| rs371122851 | 3:69,360,423 | A/G | — | likely benign |
| rs2472254088 | 3:69,362,625 | C/T | — | uncertain significance |
| rs115983374 | 3:69,367,693 | A/G | intron variant | — |
| rs6805807 | 3:69,395,073 | C/T | — | — |
| rs9310148 | 3:69,399,723 | T/G | — | — |
| rs571099996 | 3:69,399,894 | A/G | — | — |
| rs6795775 | 3:69,402,801 | C/T | regulatory region variant | — |
| rs17005647 | 3:69,406,181 | C/G | — | — |
| rs900669 | 3:69,406,802 | T/A | intron variant | — |
| rs60969945 | 3:69,417,665 | C/G | — | — |
| rs2471315361 | 3:69,434,995 | A/T | — | uncertain significance |
| rs757274828 | 3:69,435,106 | A/C | — | uncertain significance |
| rs13083679 | 3:69,435,604 | C/T | regulatory region variant | — |
| rs922948 | 3:69,442,637 | G/A | intron variant | — |
| rs6781386 | 3:69,473,754 | T/C | intron variant | — |
| rs58006784 | 3:69,480,788 | C/A | — | — |
| rs12497181 | 3:69,562,980 | G/A | intron variant | — |
| rs62252355 | 3:69,572,006 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.