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
32081	NOTCH1	rs775910009	SNP	missense variant	L/P	2446	171	0.17	249	benign	0.248	22001	likely benign	22
32082	NOTCH1	rs1564567692	SNP	missense variant	P/L	2445	241	0.24	119	benign	0.118	22001	likely benign	22
32083	NOTCH1	rs748783098	SNP	missense variant	P/S	2445	231	0.23	13	benign	0.012	16001	likely benign	16
32084	NOTCH1	rs1418965547	SNP	missense variant	V/G	2443	361	0.36	180	benign	0.179	19001	likely benign	19
32085	NOTCH1	rs768311067	SNP	missense variant	V/L	2443	1001	1	2	benign	0.001	13001	likely benign	13
32086	NOTCH1	rs768311067	SNP	missense variant	V/M	2443	331	0.33	8	benign	0.007	17001	likely benign	17
32087	NOTCH1	rs1131691402	SNP	missense variant	S/T	2439	251	0.25	11	benign	0.01	17001	likely benign	17
32088	NOTCH1	rs942055234	SNP	missense variant	S/R	2439	171	0.17	399	benign	0.398	21001	likely benign	21
32089	NOTCH1	rs199777870	SNP	missense variant	P/L	2438	691	0.69	1	benign	0	15001	likely benign	15
32090	NOTCH1	rs1163865960	SNP	missense variant	P/S	2438	411	0.41	48	benign	0.047	16001	likely benign	16

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