Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
25241	MLL2	rs778879514	SNP	missense variant	M/V	1767	51	0.05	22	benign	0.021	20001	likely benign	20
25242	MLL2	rs963946740	SNP	missense variant	E/D	1765	1	0	988	probably damaging	0.987	22001	likely benign	22
25243	MLL2	rs777604931	SNP	missense variant	S/T	1762	301	0.3	12	benign	0.011	18001	likely benign	18
25244	MLL2	rs777604931	SNP	missense variant	S/N	1762	431	0.43	2	benign	0.001	18001	likely benign	18
25245	MLL2	rs1565802308	SNP	missense variant	R/C	1759	1	0	983	probably damaging	0.982	30001	likely deleterious	30
25246	MLL2	rs908795312	SNP	missense variant	R/P	1756	41	0.04	863	possibly damaging	0.862	27001	likely benign	27
25247	MLL2	rs908795312	SNP	missense variant	R/Q	1756	61	0.06	704	possibly damaging	0.703	24001	likely benign	24
25248	MLL2	rs770835064	SNP	missense variant	R/W	1756	11	0.01	965	probably damaging	0.964	28001	likely benign	28
25249	MLL2	rs866369324	SNP	missense variant	Q/H	1755	21	0.02	276	benign	0.275	22001	likely benign	22
25250	MLL2	rs1347371008	SNP	missense variant	K/T	1753	51	0.05	992	probably damaging	0.991	25001	likely benign	25

Left 2524 2525 2526