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
1111	MYC	rs143501729	SNP	missense variant	A/E	454	1	0	15	benign	0.014	22001	likely benign	22
1112	CCND1	rs572037183	SNP	missense variant	E/K	2	141	0.14	13	benign	0.012	23001	likely benign	23
1113	CCND1	rs572037183	SNP	missense variant	E/Q	2	171	0.17	52	benign	0.051	23001	likely benign	23
1114	CCND1	rs545664320	SNP	missense variant	H/R	3	151	0.15	24	benign	0.023	21001	likely benign	21
1115	CCND1	rs1356268873	SNP	missense variant	Q/H	4	1	0	309	benign	0.308	24001	likely benign	24
1116	CCND1	rs993495966	SNP	missense variant	C/S	7	1	0	980	probably damaging	0.979	28001	likely benign	28
1117	CCND1	rs993495966	SNP	missense variant	C/R	7	1	0	995	probably damaging	0.994	31001	likely deleterious	31
1118	CCND1	rs1486252402	SNP	missense variant	C/S	7	1	0	980	probably damaging	0.979	28001	likely benign	28
1119	CCND1	rs773884084	SNP	missense variant	C/G	8	41	0.04	72	benign	0.071	24001	likely benign	24
1120	CCND1	rs1340132260	SNP	missense variant	C/Y	8	81	0.08	710	possibly damaging	0.709	25001	likely benign	25

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