BICRA
BRD4 interacting chromatin remodeling complex associated protein
Summary
Enables transcription regulator activator activity. Involved in positive regulation of DNA-templated transcription. Located in nucleus. Part of SWI/SNF complex. Implicated in Coffin-Siris syndrome 12. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants272 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2099052 | 19:48,110,625 | G/T | upstream gene variant | — |
| rs994623044 | 19:48,111,539 | G/A | — | uncertain significance |
| rs2913995 | 19:48,117,028 | T/C | regulatory region variant | — |
| rs11673468 | 19:48,129,521 | C/T | coding sequence variant | — |
| rs41374344 | 19:48,131,817 | G/A | — | — |
| rs11881441 | 19:48,142,746 | A/G | — | — |
| rs2081178 | 19:48,163,091 | T/G | — | — |
| rs2911003 | 19:48,167,935 | T/C | regulatory region variant | — |
| rs202093781 | 19:48,176,977 | T/C | — | likely benign |
| rs200233936 | 19:48,177,013 | C/T | — | likely benign |
| rs2123579791 | 19:48,179,111 | G/C | — | uncertain significance |
| rs749683547 | 19:48,179,114 | A/G | — | uncertain significance |
| rs187227564 | 19:48,179,125 | C/T | — | likely benign |
| rs375078723 | 19:48,179,138 | G/A | — | uncertain significance |
| rs765058558 | 19:48,179,160 | A/G | — | uncertain significance |
| rs1385590427 | 19:48,179,168 | C/T | — | uncertain significance |
| rs2911005 | 19:48,182,568 | C/T | — | benign |
| rs2123584339 | 19:48,182,619 | G/C | — | pathogenic |
| rs2514107655 | 19:48,182,678 | C/G | — | uncertain significance |
| rs1310999953 | 19:48,182,689 | G/A | — | uncertain significance |
| rs191148484 | 19:48,182,698 | G/A | — | likely benign |
| rs779275819 | 19:48,182,701 | G/A | — | uncertain significance |
| rs942604977 | 19:48,182,717 | C/T | — | uncertain significance |
| rs922454643 | 19:48,182,761 | A/G | — | uncertain significance |
| rs2514107813 | 19:48,182,764 | A/G | — | uncertain significance |
| rs2123584602 | 19:48,182,765 | T/G | — | uncertain significance |
| rs2123584619 | 19:48,182,777 | C/T | — | uncertain significance |
| rs4802382 | 19:48,182,787 | C/T | — | benign |
| rs1339426875 | 19:48,182,788 | G/C | — | uncertain significance |
| rs758895374 | 19:48,182,809 | C/T | — | uncertain significance |
| rs866927746 | 19:48,182,837 | C/T | — | uncertain significance |
| rs2514107981 | 19:48,182,879 | C/G | — | uncertain significance |
| rs2123584873 | 19:48,182,885 | C/T | — | uncertain significance |
| rs117898943 | 19:48,182,919 | C/T | — | benign |
| rs1599846930 | 19:48,182,942 | C/T | — | uncertain significance |
| rs2911006 | 19:48,182,946 | T/C | — | benign |
| rs2123585052 | 19:48,182,962 | C/T | — | pathogenic |
| rs2514108362 | 19:48,183,037 | G/C | — | uncertain significance |
| rs2514108437 | 19:48,183,062 | C/T | — | uncertain significance |
| rs565570206 | 19:48,183,083 | A/G | — | uncertain significance |
| rs2914438 | 19:48,183,114 | A/G | — | benign |
| rs1278557758 | 19:48,183,119 | G/C | — | uncertain significance |
| rs1478730480 | 19:48,183,149 | C/G | — | uncertain significance |
| rs2514108727 | 19:48,183,185 | T/C | — | uncertain significance |
| rs2514108733 | 19:48,183,187 | G/A | — | uncertain significance |
| rs2514108749 | 19:48,183,196 | G/C | — | uncertain significance |
| rs1973006501 | 19:48,183,224 | C/T | — | uncertain significance |
| rs374629203 | 19:48,183,234 | C/A | — | likely benign |
| rs1210103414 | 19:48,183,295 | C/T | — | likely pathogenic |
| rs748949915 | 19:48,183,328 | C/T | — | conflicting classifications of pathogenicity |
| rs1162910845 | 19:48,183,332 | A/G | — | uncertain significance |
| rs2514109040 | 19:48,183,342 | T/C | — | likely benign |
| rs141698853 | 19:48,183,364 | G/C | — | uncertain significance |
| rs1220144943 | 19:48,183,398 | C/T | — | uncertain significance |
| rs1488202419 | 19:48,183,412 | C/T | — | uncertain significance |
| rs1194693763 | 19:48,183,420 | C/T | — | likely benign |
| rs758258738 | 19:48,183,437 | T/C | — | uncertain significance |
| rs749402835 | 19:48,183,443 | C/T | — | uncertain significance |
| rs1434287792 | 19:48,183,445 | C/T | — | uncertain significance |
| rs541468081 | 19:48,183,499 | G/C | — | uncertain significance |
| rs373727053 | 19:48,183,507 | G/A | — | likely benign |
| rs2514109547 | 19:48,183,523 | C/G | — | uncertain significance |
| rs367911716 | 19:48,183,573 | C/T | — | likely benign |
| rs1458579543 | 19:48,183,589 | C/T | — | uncertain significance |
| rs1017494973 | 19:48,183,608 | C/T | — | uncertain significance |
| rs997507499 | 19:48,183,625 | A/G | — | uncertain significance |
| rs371215563 | 19:48,183,633 | G/T | — | benign |
| rs780989056 | 19:48,183,651 | C/A | — | uncertain significance |
| rs1444702735 | 19:48,183,652 | G/T | — | uncertain significance |
| rs1264388301 | 19:48,183,671 | C/G | — | uncertain significance |
| rs2514109967 | 19:48,183,719 | C/T | — | uncertain significance |
| rs1973024285 | 19:48,183,736 | C/T | — | uncertain significance |
| rs998299578 | 19:48,183,748 | G/A | — | uncertain significance |
| rs1035938 | 19:48,183,771 | C/T | synonymous variant | — |
| rs1453276046 | 19:48,183,791 | G/A | — | uncertain significance |
| rs2123587132 | 19:48,183,808 | C/A | — | uncertain significance |
| rs781498159 | 19:48,183,820 | A/G | — | uncertain significance |
| rs1272044786 | 19:48,183,826 | C/T | — | uncertain significance |
| rs759158134 | 19:48,183,856 | G/A | — | likely benign |
| rs372970799 | 19:48,183,903 | C/T | — | likely benign |
| rs1973031308 | 19:48,183,934 | C/G | — | uncertain significance |
| rs767725444 | 19:48,183,937 | C/T | — | uncertain significance |
| rs2514110617 | 19:48,183,979 | C/G | — | uncertain significance |
| rs945429331 | 19:48,184,024 | C/A | — | uncertain significance |
| rs201151265 | 19:48,184,029 | C/A | — | likely benign |
| rs757601704 | 19:48,184,037 | A/C | — | uncertain significance |
| rs779469273 | 19:48,184,041 | C/A | — | uncertain significance |
| rs1002097578 | 19:48,184,051 | C/T | — | uncertain significance |
| rs376362178 | 19:48,184,059 | C/T | — | likely benign |
| rs1973035781 | 19:48,184,066 | A/T | — | uncertain significance |
| rs1973036340 | 19:48,184,081 | C/T | — | uncertain significance |
| rs1973036670 | 19:48,184,098 | G/T | — | uncertain significance |
| rs1002065322 | 19:48,184,134 | G/C | — | benign |
| rs1474602084 | 19:48,184,146 | G/A | — | likely benign |
| rs755798126 | 19:48,184,152 | C/T | — | likely benign |
| rs1488520440 | 19:48,184,162 | G/A | — | uncertain significance |
| rs770829678 | 19:48,184,194 | C/T | — | likely benign |
| rs776784703 | 19:48,184,204 | G/A | — | uncertain significance |
| rs1433149793 | 19:48,184,216 | A/G | — | uncertain significance |
| rs934191154 | 19:48,184,223 | C/T | — | uncertain significance |
Showing 100 of 272 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.