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
23081	MLL2	rs777292389	SNP	missense variant	N/S	4572	211	0.21	160	benign	0.159	20001	likely benign	20
23082	MLL2	rs756908474	SNP	missense variant	A/T	4571	41	0.04	8	benign	0.007	21001	likely benign	21
23083	MLL2	rs200747793	SNP	missense variant	T/P	4570	141	0.14	672	possibly damaging	0.671	24001	likely benign	24
23084	MLL2	rs1009316575	SNP	missense variant	I/M	4569	11	0.01	685	possibly damaging	0.684	24001	likely benign	24
23085	MLL2	rs745652015	SNP	missense variant	I/V	4569	61	0.06	8	benign	0.007	20001	likely benign	20
23086	MLL2	rs769668980	SNP	missense variant	A/V	4568	271	0.27	2	benign	0.001	20001	likely benign	20
23087	MLL2	rs1352215113	SNP	missense variant	A/P	4568	71	0.07	1	benign	0	19001	likely benign	19
23088	MLL2	rs1171761414	SNP	missense variant	E/V	4566	1	0	691	possibly damaging	0.69	28001	likely benign	28
23089	MLL2	rs749198835	SNP	missense variant	T/M	4565	1001	1	2	benign	0.001	13001	likely benign	13
23090	MLL2	rs1317027250	SNP	missense variant	L/V	4564	51	0.05	992	probably damaging	0.991	22001	likely benign	22

Left 2308 2309 2310