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
6921	KM2TC-MLL3	rs751330761	SNP	missense variant	A/V	4308	341	0.34	7	benign	0.006	13001	likely benign	13
6922	KM2TC-MLL3	rs756354376	SNP	missense variant	A/S	4308	781	0.78	1	benign	0	1	likely benign	0
6923	KM2TC-MLL3	rs756354376	SNP	missense variant	A/T	4308	1001	1	1	benign	0	1	likely benign	0
6924	KM2TC-MLL3	rs1301639861	SNP	missense variant	P/R	4302	1	0	565	possibly damaging	0.564	26001	likely benign	26
6925	KM2TC-MLL3	rs1301639861	SNP	missense variant	P/H	4302	1	0	782	possibly damaging	0.781	26001	likely benign	26
6926	KM2TC-MLL3	rs559520719	SNP	missense variant	P/A	4302	91	0.09	113	benign	0.112	21001	likely benign	21
6927	KM2TC-MLL3	rs559520719	SNP	missense variant	P/T	4302	111	0.11	31	benign	0.03	22001	likely benign	22
6928	KM2TC-MLL3	rs1299251851	SNP	missense variant	P/A	4301	51	0.05	366	benign	0.365	20001	likely benign	20
6929	KM2TC-MLL3	rs1362399833	SNP	missense variant	S/C	4300	1	0	988	probably damaging	0.987	27001	likely benign	27
6930	KM2TC-MLL3	rs199880787	SNP	missense variant	S/A	4300	51	0.05	830	possibly damaging	0.829	26001	likely benign	26

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