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
29821	SMAD4	rs1343555503	SNP	missense variant	S/N	271	261	0.26	4	benign	0.003	21001	likely benign	21
29822	SMAD4	rs1282145977	SNP	missense variant	T/S	273	101	0.1	7	benign	0.006	17001	likely benign	17
29823	SMAD4	rs751860447	SNP	missense variant	A/T	274	61	0.06	8	benign	0.007	22001	likely benign	22
29824	SMAD4	rs1229812463	SNP	missense variant	Y/F	276	301	0.3	424	benign	0.423	22001	likely benign	22
29825	SMAD4	rs1555685960	SNP	missense variant	T/A	277	71	0.07	991	probably damaging	0.99	21001	likely benign	21
29826	SMAD4	rs1257577085	SNP	missense variant	P/T	278	41	0.04	999	probably damaging	0.998	21001	likely benign	21
29827	SMAD4	rs1568206174	SNP	missense variant	P/L	281	11	0.01	999	probably damaging	0.998	22001	likely benign	22
29828	SMAD4	rs1555685962	SNP	missense variant	H/P	282	391	0.39	994	probably damaging	0.993	22001	likely benign	22
29829	SMAD4	rs750111831	SNP	missense variant	G/S	286	11	0.01	1000	probably damaging	0.999	23001	likely benign	23
29830	SMAD4	rs1568206180	SNP	missense variant	H/R	287	1001	1	984	probably damaging	0.983	20001	likely benign	20

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