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
23521	MLL2	rs527255553	SNP	missense variant	P/L	4048	11	0.01	40	benign	0.039	18001	likely benign	18
23522	MLL2	rs527255553	SNP	missense variant	P/R	4048	11	0.01	72	benign	0.071	18001	likely benign	18
23523	MLL2	rs1184355553	SNP	missense variant	P/S	4048	221	0.22	1	benign	0	10001	likely benign	10
23524	MLL2	rs587778478	SNP	missense variant	G/R	4047	11	0.01	16	benign	0.015	21001	likely benign	21
23525	MLL2	rs750872313	SNP	missense variant	G/E	4046	11	0.01	11	benign	0.01	18001	likely benign	18
23526	MLL2	rs1565775707	SNP	missense variant	G/R	4046	11	0.01	11	benign	0.01	17001	likely benign	17
23527	MLL2	rs1446650180	SNP	missense variant	Q/R	4045	1	0	256	benign	0.255	21001	likely benign	21
23528	MLL2	rs548090054	SNP	missense variant	Q/E	4045	1	0	79	benign	0.078	21001	likely benign	21
23529	MLL2	rs779579389	SNP	missense variant	T/I	4043	111	0.11	4	benign	0.003	17001	likely benign	17
23530	MLL2	rs748772041	SNP	missense variant	T/P	4043	151	0.15	1	benign	0	12001	likely benign	12

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