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
24871	MLL2	rs772930636	SNP	missense variant	A/T	2220	1001	1	1	benign	0	4001	likely benign	4
24872	MLL2	rs1221290632	SNP	missense variant	G/E	2219	51	0.05	743	possibly damaging	0.742	22001	likely benign	22
24873	MLL2	rs1278872705	SNP	missense variant	P/L	2218	11	0.01	187	benign	0.186	22001	likely benign	22
24874	MLL2	rs760319994	SNP	missense variant	P/S	2218	51	0.05	4	benign	0.003	14001	likely benign	14
24875	MLL2	rs1201197190	SNP	missense variant	R/H	2217	71	0.07	4	benign	0.003	18001	likely benign	18
24876	MLL2	rs770789888	SNP	missense variant	R/C	2217	1	0	586	possibly damaging	0.585	25001	likely benign	25
24877	MLL2	rs1466593517	SNP	missense variant	S/F	2216	211	0.21	192	benign	0.191	20001	likely benign	20
24878	MLL2	rs888575024	SNP	missense variant	S/P	2216	321	0.32	64	benign	0.063	14001	likely benign	14
24879	MLL2	rs200080744	SNP	missense variant	S/T	2215	181	0.18	2	benign	0.001	11001	likely benign	11
24880	MLL2	rs1193338123	SNP	missense variant	A/G	2214	61	0.06	26	benign	0.025	14001	likely benign	14

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