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
26511	MLL2	rs1432323879	SNP	missense variant	V/A	97	731	0.73	1	benign	0	10001	likely benign	10
26512	MLL2	rs375614893	SNP	missense variant	V/L	97	451	0.45	1	benign	0	14001	likely benign	14
26513	MLL2	rs763699658	SNP	missense variant	V/L	96	301	0.3	1	benign	0	15001	likely benign	15
26514	MLL2	rs763699658	SNP	missense variant	V/M	96	91	0.09	24	benign	0.023	16001	likely benign	16
26515	MLL2	rs766805522	SNP	missense variant	C/Y	94	81	0.08	8	benign	0.007	18001	likely benign	18
26516	MLL2	rs1301033353	SNP	missense variant	R/Q	93	171	0.17	1	benign	0	14001	likely benign	14
26517	MLL2	rs781092896	SNP	missense variant	R/W	93	1	0	1	benign	0	23001	likely benign	23
26518	MLL2	rs750283044	SNP	missense variant	P/A	92	31	0.03	992	probably damaging	0.991	24001	likely benign	24
26519	MLL2	rs780096090	SNP	missense variant	R/L	84	101	0.1	45	benign	0.044	22001	likely benign	22
26520	MLL2	rs780096090	SNP	missense variant	R/H	84	211	0.21	7	benign	0.006	22001	likely benign	22

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