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
1191	CCND1	rs866931401	SNP	missense variant	R/Q	133	401	0.4	1	benign	0	19001	likely benign	19
1192	CCND1	rs866931401	SNP	missense variant	R/L	133	211	0.21	1	benign	0	20001	likely benign	20
1193	CCND1	rs765498502	SNP	missense variant	P/S	134	161	0.16	55	benign	0.054	23001	likely benign	23
1194	CCND1	rs763443319	SNP	missense variant	E/K	135	461	0.46	4	benign	0.003	23001	likely benign	23
1195	CCND1	rs764335132	SNP	missense variant	E/V	135	101	0.1	15	benign	0.014	23001	likely benign	23
1196	CCND1	rs1184664065	SNP	missense variant	E/A	136	11	0.01	433	benign	0.432	27001	likely benign	27
1197	CCND1	rs900779300	SNP	missense variant	E/D	136	161	0.16	16	benign	0.015	22001	likely benign	22
1198	CCND1	rs752157015	SNP	missense variant	L/M	137	41	0.04	904	possibly damaging	0.903	24001	likely benign	24
1199	CCND1	rs1268871232	SNP	missense variant	Q/H	139	31	0.03	4	benign	0.003	23001	likely benign	23
1200	CCND1	rs1260695584	SNP	missense variant	L/F	143	71	0.07	332	benign	0.331	21001	likely benign	21

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