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
10021	KM2TC-MLL3	rs754743885	SNP	missense variant	Q/L	103	111	0.11	41	benign	0.04	14001	likely benign	14
10022	KM2TC-MLL3	rs1341155361	SNP	missense variant	S/N	101	181	0.18	2	benign	0.001	13001	likely benign	13
10023	KM2TC-MLL3	rs751799633	SNP	missense variant	S/C	101	31	0.03	431	benign	0.43	22001	likely benign	22
10024	KM2TC-MLL3	rs1313266616	SNP	missense variant	N/D	100	691	0.69	19	benign	0.018	14001	likely benign	14
10025	KM2TC-MLL3	rs1358968676	SNP	missense variant	D/G	99	21	0.02	147	benign	0.146	23001	likely benign	23
10026	KM2TC-MLL3	rs1358968676	SNP	missense variant	D/A	99	11	0.01	82	benign	0.081	23001	likely benign	23
10027	KM2TC-MLL3	rs757337368	SNP	missense variant	V/A	98	351	0.35	4	benign	0.003	7001	likely benign	7
10028	KM2TC-MLL3	rs987201117	SNP	missense variant	V/M	98	21	0.02	549	possibly damaging	0.548	22001	likely benign	22
10029	KM2TC-MLL3	rs756646196	SNP	missense variant	E/V	95	191	0.19	117	benign	0.116	22001	likely benign	22
10030	KM2TC-MLL3	rs780491145	SNP	missense variant	D/A	93	21	0.02	197	benign	0.196	23001	likely benign	23

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