Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
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id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
25751	MLL2	rs1382796110	SNP	missense variant	V/I	1033	21	0.02	1	benign	0	16001	likely benign	16
25752	MLL2	rs371296793	SNP	missense variant	S/C	1031	1	0	432	benign	0.431	21001	likely benign	21
25753	MLL2	rs374230943	SNP	missense variant	H/R	1030	81	0.08	1	benign	0	11001	likely benign	11
25754	MLL2	rs752016184	SNP	missense variant	H/Y	1030	21	0.02	1	benign	0	20001	likely benign	20
25755	MLL2	rs961754523	SNP	missense variant	L/F	1028	1	0	8	benign	0.007	20001	likely benign	20
25756	MLL2	rs1453591888	SNP	missense variant	L/F	1027	31	0.03	2	benign	0.001	16001	likely benign	16
25757	MLL2	rs757409344	SNP	missense variant	P/S	1026	1	0	71	benign	0.07	21001	likely benign	21
25758	MLL2	rs746163543	SNP	missense variant	S/L	1025	1	0	30	benign	0.029	22001	likely benign	22
25759	MLL2	rs770148458	SNP	missense variant	S/P	1025	101	0.1	285	benign	0.284	20001	likely benign	20
25760	MLL2	rs757756934	SNP	missense variant	C/R	1024	21	0.02	4	benign	0.003	22001	likely benign	22

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