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
23261	MLL2	rs181733689	SNP	missense variant	P/A	4349	261	0.26	40	benign	0.039	17001	likely benign	17
23262	MLL2	rs181733689	SNP	missense variant	P/T	4349	11	0.01	7	benign	0.006	22001	likely benign	22
23263	MLL2	rs777614562	SNP	missense variant	G/V	4348	1	0	40	benign	0.039	16001	likely benign	16
23264	MLL2	rs1328256473	SNP	missense variant	G/R	4348	1	0	217	benign	0.216	21001	likely benign	21
23265	MLL2	rs746765275	SNP	missense variant	P/L	4346	1	0	6	benign	0.005	21001	likely benign	21
23266	MLL2	rs1194839707	SNP	missense variant	P/S	4346	101	0.1	2	benign	0.001	11001	likely benign	11
23267	MLL2	rs922101505	SNP	missense variant	K/N	4345	11	0.01	1	benign	0	8001	likely benign	8
23268	MLL2	rs777630263	SNP	missense variant	K/R	4345	241	0.24	1	benign	0	12001	likely benign	12
23269	MLL2	rs1274991344	SNP	missense variant	P/L	4344	31	0.03	6	benign	0.005	22001	likely benign	22
23270	MLL2	rs1394926925	SNP	missense variant	T/N	4343	51	0.05	8	benign	0.007	19001	likely benign	19

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