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
23801	MLL2	rs201702616	SNP	missense variant	G/A	3660	131	0.13	4	benign	0.003	16001	likely benign	16
23802	MLL2	rs201702616	SNP	missense variant	G/E	3660	1	0	246	benign	0.245	22001	likely benign	22
23803	MLL2	rs367910969	SNP	missense variant	P/S	3659	11	0.01	550	possibly damaging	0.549	24001	likely benign	24
23804	MLL2	rs367910969	SNP	missense variant	P/T	3659	11	0.01	703	possibly damaging	0.702	24001	likely benign	24
23805	MLL2	rs767668562	SNP	missense variant	T/I	3658	31	0.03	7	benign	0.006	23001	likely benign	23
23806	MLL2	rs750556938	SNP	missense variant	L/V	3657	81	0.08	198	benign	0.197	15001	likely benign	15
23807	MLL2	rs1232636989	SNP	missense variant	R/P	3656	1	0	954	probably damaging	0.953	25001	likely benign	25
23808	MLL2	rs1232636989	SNP	missense variant	R/H	3656	1	0	74	benign	0.073	23001	likely benign	23
23809	MLL2	rs201283589	SNP	missense variant	R/C	3656	1	0	972	probably damaging	0.971	27001	likely benign	27
23810	MLL2	rs768831474	SNP	missense variant	L/R	3655	1	0	841	possibly damaging	0.84	24001	likely benign	24

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