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
16371	PIK3R1	rs757620613	SNP	missense variant	I/M	182	51	0.05	55	benign	0.054	22001	likely benign	22
16372	PIK3R1	rs1299498656	SNP	missense variant	K/E	186	71	0.07	18	benign	0.017	23001	likely benign	23
16373	EGFR	rs767259994	SNP	missense variant	N/S	3	881	0.88	1	benign	0	18001	likely benign	18
16374	EGFR	rs1562752927	SNP	missense variant	N/K	4	31	0.03	63	benign	0.062	22001	likely benign	22
16375	EGFR	rs760228905	SNP	missense variant	E/K	6	11	0.01	744	possibly damaging	0.743	25001	likely benign	25
16376	EGFR	rs763572530	SNP	missense variant	E/A	6	11	0.01	973	probably damaging	0.972	26001	likely benign	26
16377	EGFR	rs369580836	SNP	missense variant	Q/P	18	521	0.52	12	benign	0.011	20001	likely benign	20
16378	EGFR	rs369580836	SNP	missense variant	Q/R	18	221	0.22	276	benign	0.275	21001	likely benign	21
16379	EGFR	rs1269583681	SNP	missense variant	N/K	20	81	0.08	93	benign	0.092	10001	likely benign	10
16380	EGFR	rs778638117	SNP	missense variant	L/I	23	11	0.01	831	possibly damaging	0.83	25001	likely benign	25

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