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
8681	KM2TC-MLL3	rs191189760	SNP	missense variant	C/S	1953	211	0.21	21	benign	0.02	16001	likely benign	16
8682	KM2TC-MLL3	rs781220804	SNP	missense variant	D/N	1951	11	0.01	440	benign	0.439	23001	likely benign	23
8683	KM2TC-MLL3	rs745832908	SNP	missense variant	P/L	1948	1	0	739	possibly damaging	0.738	25001	likely benign	25
8684	KM2TC-MLL3	rs756054369	SNP	missense variant	S/Y	1947	1	0	997	probably damaging	0.996	25001	likely benign	25
8685	KM2TC-MLL3	rs1563290134	SNP	missense variant	P/S	1946	51	0.05	853	possibly damaging	0.852	23001	likely benign	23
8686	KM2TC-MLL3	rs1342962740	SNP	missense variant	R/K	1945	21	0.02	971	probably damaging	0.97	24001	likely benign	24
8687	KM2TC-MLL3	rs779879693	SNP	missense variant	N/S	1944	851	0.85	1	benign	0	1	likely benign	0
8688	KM2TC-MLL3	rs748650886	SNP	missense variant	N/Y	1944	91	0.09	203	benign	0.202	17001	likely benign	17
8689	KM2TC-MLL3	rs1213064306	SNP	missense variant	A/T	1943	191	0.19	2	benign	0.001	14001	likely benign	14
8690	KM2TC-MLL3	rs772288933	SNP	missense variant	T/I	1942	81	0.08	76	benign	0.075	15001	likely benign	15

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