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
8581	KM2TC-MLL3	rs781608784	SNP	missense variant	E/G	2073	21	0.02	995	probably damaging	0.994	26001	likely benign	26
8582	KM2TC-MLL3	rs1292477105	SNP	missense variant	Y/C	2072	1	0	998	probably damaging	0.997	27001	likely benign	27
8583	KM2TC-MLL3	rs1238297866	SNP	missense variant	P/A	2071	91	0.09	142	benign	0.141	17001	likely benign	17
8584	KM2TC-MLL3	rs950653826	SNP	missense variant	D/E	2070	1	0	837	possibly damaging	0.836	23001	likely benign	23
8585	KM2TC-MLL3	rs587778498	SNP	missense variant	R/Q	2066	31	0.03	993	probably damaging	0.992	23001	likely benign	23
8586	KM2TC-MLL3	rs367655701	SNP	missense variant	S/L	2064	141	0.14	108	benign	0.107	21001	likely benign	21
8587	KM2TC-MLL3	rs1179787171	SNP	missense variant	A/V	2063	41	0.04	40	benign	0.039	23001	likely benign	23
8588	KM2TC-MLL3	rs1381665445	SNP	missense variant	A/T	2063	601	0.6	1	benign	0	8001	likely benign	8
8589	KM2TC-MLL3	rs756421421	SNP	missense variant	Q/R	2062	181	0.18	56	benign	0.055	14001	likely benign	14
8590	KM2TC-MLL3	rs756421421	SNP	missense variant	Q/P	2062	371	0.37	101	benign	0.1	14001	likely benign	14

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