Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
9381	KM2TC-MLL3	rs1320275944	SNP	missense variant	P/L	891	1	0	998	probably damaging	0.997	33001	likely deleterious	33
9382	KM2TC-MLL3	rs1198569820	SNP	missense variant	S/F	888	1	0	992	probably damaging	0.991	31001	likely deleterious	31
9383	KM2TC-MLL3	rs151069596	SNP	missense variant	S/A	888	11	0.01	953	probably damaging	0.952	25001	likely benign	25
9384	KM2TC-MLL3	rs151069596	SNP	missense variant	S/T	888	21	0.02	953	probably damaging	0.952	24001	likely benign	24
9385	KM2TC-MLL3	rs112773078	SNP	missense variant	R/H	886	1	0	680	possibly damaging	0.679	27001	likely benign	27
9386	KM2TC-MLL3	rs199796679	SNP	missense variant	R/C	886	1	0	989	probably damaging	0.988	33001	likely deleterious	33
9387	KM2TC-MLL3	rs1232382756	SNP	missense variant	G/V	885	1	0	1000	probably damaging	0.999	29001	likely benign	29
9388	KM2TC-MLL3	rs377179307	SNP	missense variant	K/R	883	491	0.49	58	benign	0.057	22001	likely benign	22
9389	KM2TC-MLL3	rs199839047	SNP	missense variant	I/T	882	11	0.01	797	possibly damaging	0.796	26001	likely benign	26
9390	KM2TC-MLL3	rs1432496136	SNP	missense variant	I/V	882	111	0.11	295	benign	0.294	18001	likely benign	18

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