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
29831	SMAD4	rs1451329701	SNP	missense variant	Q/R	289	191	0.19	975	probably damaging	0.974	22001	likely benign	22
29832	SMAD4	rs755770046	SNP	missense variant	H/P	290	81	0.08	2	benign	0.001	24001	likely benign	24
29833	SMAD4	rs863224733	SNP	missense variant	H/Y	291	11	0.01	424	benign	0.423	23001	likely benign	23
29834	SMAD4	rs779583608	SNP	missense variant	H/P	291	21	0.02	2	benign	0.001	24001	likely benign	24
29835	SMAD4	rs786201404	SNP	missense variant	P/L	292	11	0.01	304	benign	0.303	21001	likely benign	21
29836	SMAD4	rs1555685965	SNP	missense variant	P/S	293	11	0.01	998	probably damaging	0.997	23001	likely benign	23
29837	SMAD4	rs7238500	SNP	missense variant	M/V	294	151	0.15	20	benign	0.019	17001	likely benign	17
29838	SMAD4	rs1167543544	SNP	missense variant	P/A	295	831	0.83	63	benign	0.062	15001	likely benign	15
29839	SMAD4	rs370176106	SNP	missense variant	P/Q	295	311	0.31	16	benign	0.015	19001	likely benign	19
29840	SMAD4	rs370176106	SNP	missense variant	P/R	295	201	0.2	306	benign	0.305	20001	likely benign	20

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