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
71	TP53	rs55819519	SNP	missense variant	R/L	290	61	0.06	16	benign	0.015	3001	likely benign	3
72	TP53	rs55819519	SNP	missense variant	R/P	290	11	0.01	864	possibly damaging	0.863	13001	likely benign	13
73	TP53	rs55819519	SNP	missense variant	R/H	290	351	0.35	6	benign	0.005	1001	likely benign	1
74	TP53	rs770374782	SNP	missense variant	R/C	290	1	0	878	possibly damaging	0.877	26001	likely benign	26
75	TP53	rs770374782	SNP	missense variant	R/G	290	51	0.05	647	possibly damaging	0.646	22001	likely benign	22
76	TP53	rs1555525154	SNP	missense variant	L/V	289	41	0.04	1	benign	0	12001	likely benign	12
77	TP53	rs748891343	SNP	missense variant	E/D	287	651	0.65	28	benign	0.027	4001	likely benign	4
78	TP53	rs587782006	SNP	missense variant	E/K	287	21	0.02	224	benign	0.223	23001	likely benign	23
79	TP53	rs1057519985	SNP	missense variant	E/V	286	1	0	710	possibly damaging	0.709	32001	likely deleterious	32
80	TP53	rs1057519985	SNP	missense variant	E/G	286	1	0	991	probably damaging	0.99	32001	likely deleterious	32

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