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
16251	NF1	rs375468032	SNP	missense variant	H/Q	12	211	0.21	878	possibly damaging	0.877	20001	likely benign	20
16252	NF1	rs876658554	SNP	missense variant	S/T	15	301	0.3	172	benign	0.171	20001	likely benign	20
16253	NF1	rs876658554	SNP	missense variant	S/P	15	11	0.01	109	benign	0.108	24001	likely benign	24
16254	NF1	rs772707560	SNP	missense variant	P/S	16	401	0.4	121	benign	0.12	19001	likely benign	19
16255	NF1	rs764508546	SNP	missense variant	P/S	17	441	0.44	85	benign	0.084	18001	likely benign	18
16256	NF1	rs1405312220	SNP	missense variant	Y/H	19	241	0.24	109	benign	0.108	23001	likely benign	23
16257	NF1	rs786203443	SNP	missense variant	Q/E	20	11	0.01	883	possibly damaging	0.882	24001	likely benign	24
16258	NF1	rs201824349	SNP	missense variant	Y/F	23	361	0.36	13	benign	0.012	22001	likely benign	22
16259	NF1	rs955074155	SNP	missense variant	L/M	24	31	0.03	998	probably damaging	0.997	23001	likely benign	23
16260	NF1	rs78610439	SNP	missense variant	L/F	32	1	0	1001	probably damaging	1	17001	likely benign	17

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