BRK1
BRICK1 subunit of SCAR/WAVE actin nucleating complex
Summary
Enables identical protein binding activity. Contributes to small GTPase binding activity. Involved in Rac protein signal transduction and positive regulation of cellular component organization. Located in extracellular exosome. Part of SCAR complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113153120 | 3:10,156,398 | G/A | — | benign |
| rs112509186 | 3:10,156,533 | A/G | — | benign |
| rs139538004 | 3:10,156,783 | G/C | — | benign |
| rs67852463 | 3:10,157,205 | G/C | — | benign |
| rs7645667 | 3:10,157,337 | C/A | — | benign |
| rs7645759 | 3:10,157,368 | C/T | — | benign |
| rs28532206 | 3:10,157,598 | C/A | — | benign |
| rs17032414 | 3:10,158,302 | C/G | — | benign |
| rs41464050 | 3:10,158,393 | A/G | — | benign |
| rs574131793 | 3:10,158,457 | G/T | — | — |
| rs145753279 | 3:10,159,796 | G/A | — | benign |
| rs60172687 | 3:10,159,798 | A/G | — | benign |
| rs1177674519 | 3:10,159,936 | C/A | — | benign |
| rs73117481 | 3:10,160,132 | C/T | — | benign |
| rs6776176 | 3:10,160,259 | T/C | — | benign |
| rs902058438 | 3:10,160,827 | C/A | — | benign |
| rs811907 | 3:10,160,891 | A/G | — | benign |
| rs111613623 | 3:10,161,115 | C/G | — | benign |
| rs9811908 | 3:10,161,405 | G/T | — | benign |
| rs67626468 | 3:10,161,518 | C/A | — | benign |
| rs73117489 | 3:10,162,873 | G/T | — | benign |
| rs148566381 | 3:10,163,243 | G/T | — | — |
| rs111998160 | 3:10,163,438 | C/T | — | benign |
| rs112180322 | 3:10,163,659 | C/T | — | benign |
| rs113378528 | 3:10,163,725 | C/A | — | benign |
| rs113848414 | 3:10,163,733 | T/C | — | benign |
| rs192137741 | 3:10,163,793 | G/A | — | benign |
| rs183395002 | 3:10,163,794 | T/G | — | benign |
| rs57268864 | 3:10,164,233 | C/A | — | benign |
| rs62245550 | 3:10,164,280 | T/C | — | benign |
| rs58862481 | 3:10,164,308 | G/A | — | benign |
| rs59074548 | 3:10,164,347 | G/C | — | benign |
| rs3774208 | 3:10,164,722 | T/G | — | benign |
| rs6783705 | 3:10,164,783 | A/G | — | benign |
| rs11710607 | 3:10,165,212 | C/T | — | benign |
| rs13433886 | 3:10,165,264 | G/A | — | benign |
| rs12714851 | 3:10,165,301 | A/G | — | benign |
| rs76647486 | 3:10,165,318 | T/C | — | benign |
| rs181330820 | 3:10,165,319 | T/C | — | benign |
| rs71623083 | 3:10,165,322 | G/C | — | benign |
| rs13085505 | 3:10,165,325 | A/G | — | benign |
| rs12714852 | 3:10,165,332 | A/C | — | benign |
| rs149128821 | 3:10,165,342 | T/A | — | benign |
| rs190910699 | 3:10,165,565 | A/G | — | benign |
| rs111806809 | 3:10,165,698 | T/C | — | benign |
| rs68013239 | 3:10,165,711 | G/T | — | benign |
| rs68121641 | 3:10,165,845 | T/A | — | benign |
| rs111284032 | 3:10,165,909 | C/T | — | benign |
| rs111708820 | 3:10,165,939 | C/T | — | benign |
| rs67342818 | 3:10,166,406 | G/A | — | benign |
| rs73119768 | 3:10,166,419 | T/C | — | benign |
| rs66514627 | 3:10,166,632 | A/C | — | benign |
| rs111560858 | 3:10,166,845 | G/A | — | benign |
| rs113268531 | 3:10,167,069 | A/G | — | benign |
| rs17032426 | 3:10,167,112 | G/A | — | benign |
| rs67667957 | 3:10,167,264 | G/C | — | benign |
| rs56087600 | 3:10,167,576 | T/A | — | benign |
| rs148406892 | 3:10,167,671 | A/G | — | benign |
| rs56274701 | 3:10,167,790 | G/A | — | benign |
| rs6785976 | 3:10,168,647 | T/C | — | benign |
| rs6442154 | 3:10,168,785 | T/C | — | benign |
| rs6797536 | 3:10,168,802 | A/G | — | benign |
| rs3894320 | 3:10,168,864 | A/C | — | benign |
| rs3894321 | 3:10,168,892 | T/G | — | benign |
| rs77267396 | 3:10,168,905 | C/T | — | benign |
| rs3894322 | 3:10,168,965 | G/A | — | benign |
| rs3894323 | 3:10,168,967 | G/A | — | benign |
| rs143422862 | 3:10,169,011 | C/T | — | benign |
| rs3894324 | 3:10,169,114 | G/A | — | benign |
| rs67439440 | 3:10,169,503 | C/T | — | benign |
| rs58396257 | 3:10,169,556 | A/T | — | benign |
| rs59132826 | 3:10,169,725 | G/A | — | benign |
| rs58223482 | 3:10,169,746 | G/C | — | benign |
| rs17032440 | 3:10,169,819 | G/T | — | benign |
| rs60897691 | 3:10,170,029 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.