BIRC6

baculoviral IAP repeat containing 6

Summary

This gene encodes a protein with a BIR (baculoviral inhibition of apoptosis protein repeat) domain and a UBCc (ubiquitin-conjugating enzyme E2, catalytic) domain. This protein inhibits apoptosis by facilitating the degradation of apoptotic proteins by ubiquitination. [provided by RefSeq, Jul 2008]

Known Variants292 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs767313571	2:32,582,239	G/T	—	uncertain significance
rs115758817	2:32,582,241	T/C	—	benign
rs763581869	2:32,582,248	G/A	—	uncertain significance
rs1178820415	2:32,582,252	C/T	—	uncertain significance
rs1420745785	2:32,582,309	G/A	—	uncertain significance
rs1246597140	2:32,582,347	G/C	—	uncertain significance
rs1299473626	2:32,582,389	G/C	—	uncertain significance
rs1023435711	2:32,582,411	G/A	—	uncertain significance
rs542930045	2:32,602,829	G/A	—	uncertain significance
rs150251309	2:32,613,854	T/C	—	likely benign
rs367862570	2:32,620,579	C/G	—	uncertain significance
rs376424313	2:32,620,624	G/A	—	uncertain significance
rs774500693	2:32,626,354	C/G	—	uncertain significance
rs545030293	2:32,626,374	C/T	—	uncertain significance
rs781741200	2:32,626,443	A/G	—	uncertain significance
rs1157435345	2:32,626,601	C/T	—	uncertain significance
rs2468039233	2:32,626,603	A/C	—	uncertain significance
rs780370959	2:32,631,589	G/C	—	uncertain significance
rs144006143	2:32,639,913	A/G	—	likely benign
rs2468667636	2:32,639,957	A/G	—	uncertain significance
rs781505679	2:32,639,980	A/C	—	uncertain significance
rs777391340	2:32,640,005	G/A	—	uncertain significance
rs150426823	2:32,640,038	A/C	—	likely benign
rs146405716	2:32,640,173	A/G	—	uncertain significance
rs200120740	2:32,640,240	A/C	—	uncertain significance
rs148244969	2:32,640,243	G/A	—	likely benign
rs901755465	2:32,640,322	A/C	—	uncertain significance
rs373199724	2:32,640,341	G/C	—	uncertain significance
rs2042277195	2:32,640,376	G/C	—	uncertain significance
rs34417238	2:32,640,396	A/G	—	benign
rs536388317	2:32,640,450	C/A	—	uncertain significance
rs2468693670	2:32,640,472	A/G	—	uncertain significance
rs1411052405	2:32,640,584	G/A	—	uncertain significance
rs758442904	2:32,640,592	T/G	—	uncertain significance
rs767484780	2:32,640,694	A/C	—	benign
rs2042309370	2:32,640,731	T/C	—	uncertain significance
rs144578684	2:32,640,782	A/G	—	benign
rs776144854	2:32,640,830	A/G	—	uncertain significance
rs772164177	2:32,640,908	A/G	—	uncertain significance
rs779941528	2:32,640,917	A/G	—	uncertain significance
rs768566974	2:32,640,925	A/G	—	uncertain significance
rs973796920	2:32,640,937	A/G	—	uncertain significance
rs780140402	2:32,640,991	A/G	—	likely benign
rs144184005	2:32,641,041	G/A	—	likely benign
rs562418075	2:32,641,203	C/G	—	likely benign
rs375342023	2:32,654,247	C/A	—	uncertain significance
rs763836246	2:32,654,250	G/T	—	uncertain significance
rs757908834	2:32,654,274	T/C	—	uncertain significance
rs2469306908	2:32,654,318	G/C	—	uncertain significance
rs145516075	2:32,655,985	A/G	—	likely benign
rs375637621	2:32,655,998	C/T	—	uncertain significance
rs2469398148	2:32,656,134	G/A	—	uncertain significance
rs150059343	2:32,656,153	C/T	—	benign
rs2044380980	2:32,658,783	A/G	—	uncertain significance
rs36065012	2:32,658,787	T/C	—	benign
rs770603173	2:32,658,810	A/G	—	uncertain significance
rs2044383880	2:32,658,815	C/T	—	uncertain significance
rs2044388164	2:32,658,861	G/A	—	uncertain significance
rs138022319	2:32,660,600	C/T	—	uncertain significance
rs1247739084	2:32,660,615	A/G	—	uncertain significance
rs2044605704	2:32,660,648	C/G	—	uncertain significance
rs535740674	2:32,661,111	T/G	—	likely benign
rs1186920650	2:32,661,127	G/T	—	uncertain significance
rs1044631354	2:32,661,128	A/T	—	uncertain significance
rs758242609	2:32,661,177	G/A	—	uncertain significance
rs910921413	2:32,661,203	A/G	—	likely benign
rs143158059	2:32,662,647	C/T	intron variant	—
rs2469823279	2:32,664,615	T/C	—	uncertain significance
rs185648465	2:32,664,636	G/A	—	uncertain significance
rs190360702	2:32,664,660	G/T	—	benign
rs2469828797	2:32,664,716	T/G	—	uncertain significance
rs41291167	2:32,666,411	C/T	—	benign
rs781761645	2:32,666,517	A/G	—	association
rs2469960215	2:32,667,203	A/C	—	uncertain significance
rs72867263	2:32,667,216	A/T	—	benign
rs34139419	2:32,667,289	C/T	—	benign
rs61735955	2:32,667,429	C/A	—	benign
rs185120003	2:32,667,437	T/A	—	uncertain significance
rs745552245	2:32,667,447	A/G	—	uncertain significance
rs150284362	2:32,667,454	G/A	—	uncertain significance
rs61754194	2:32,668,631	A/G	—	benign
rs1480880974	2:32,670,714	A/G	—	uncertain significance
rs2470329756	2:32,673,868	G/T	—	uncertain significance
rs150651833	2:32,673,884	A/G	—	benign
rs35205055	2:32,678,904	T/A	—	benign
rs2470555249	2:32,678,939	T/C	—	uncertain significance
rs200937433	2:32,678,962	A/T	—	uncertain significance
rs1010321798	2:32,688,442	A/G	—	uncertain significance
rs2471077138	2:32,688,448	A/G	—	uncertain significance
rs374463654	2:32,689,650	T/C	—	uncertain significance
rs367768129	2:32,689,759	A/T	—	likely benign
rs2471140005	2:32,689,812	A/G	—	uncertain significance
rs2471140658	2:32,689,824	G/C	—	uncertain significance
rs61757640	2:32,689,829	G/A	—	benign
rs758278751	2:32,689,833	T/C	—	uncertain significance
rs34906338	2:32,689,838	C/G	—	benign
rs61754195	2:32,689,842	C/T	—	benign
rs746208857	2:32,689,861	A/G	—	likely benign
rs1258242981	2:32,689,863	A/C	—	uncertain significance
rs2471143517	2:32,689,883	T/C	—	uncertain significance

Showing 100 of 292 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.