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
27721	XBP1	rs1441768634	SNP	missense variant	P/S	215	1001	1	1	benign	0	6001	likely benign	6
27722	XBP1	rs1179342020	SNP	missense variant	P/S	213	591	0.59	8	benign	0.007	11001	likely benign	11
27723	XBP1	rs1316067207	SNP	missense variant	P/S	211	921	0.92	86	benign	0.085	12001	likely benign	12
27724	XBP1	rs112130171	SNP	missense variant	K/I	209	1	0	550	possibly damaging	0.549	23001	likely benign	23
27725	XBP1	rs112130171	SNP	missense variant	K/R	209	751	0.75	6	benign	0.005	14001	likely benign	14
27726	XBP1	rs1398262920	SNP	missense variant	K/E	209	21	0.02	155	benign	0.154	13001	likely benign	13
27727	XBP1	rs1331206144	SNP	missense variant	F/L	207	101	0.1	179	benign	0.178	13001	likely benign	13
27728	XBP1	rs976661793	SNP	missense variant	M/I	206	281	0.28	195	benign	0.194	24001	likely benign	24
27729	XBP1	rs1334441820	SNP	missense variant	M/T	206	81	0.08	497	possibly damaging	0.496	28001	likely benign	28
27730	XBP1	rs1411043603	SNP	missense variant	M/L	206	991	0.99	6	benign	0.005	12001	likely benign	12

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