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
1131	CCND1	rs2220247	SNP	missense variant	A/T	30	411	0.41	4	benign	0.003	22001	likely benign	22
1132	CCND1	rs2220247	SNP	missense variant	A/S	30	421	0.42	12	benign	0.011	22001	likely benign	22
1133	CCND1	rs1415272481	SNP	missense variant	A/D	30	41	0.04	590	possibly damaging	0.589	26001	likely benign	26
1134	CCND1	rs746088878	SNP	missense variant	E/K	36	41	0.04	133	benign	0.132	26001	likely benign	26
1135	CCND1	rs1482952019	SNP	missense variant	E/D	36	401	0.4	8	benign	0.007	22001	likely benign	22
1136	CCND1	rs1263446681	SNP	missense variant	T/S	37	31	0.03	11	benign	0.01	23001	likely benign	23
1137	CCND1	rs780366497	SNP	missense variant	C/W	38	21	0.02	952	probably damaging	0.951	27001	likely benign	27
1138	CCND1	rs749614691	SNP	missense variant	S/L	41	131	0.13	302	benign	0.301	23001	likely benign	23
1139	CCND1	rs1173840555	SNP	missense variant	F/L	45	21	0.02	88	benign	0.087	24001	likely benign	24
1140	CCND1	rs747665638	SNP	missense variant	K/E	46	131	0.13	76	benign	0.075	23001	likely benign	23

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