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
24581	MLL2	rs761550628	SNP	missense variant	P/T	2550	11	0.01	997	probably damaging	0.996	24001	likely benign	24
24582	MLL2	rs767335708	SNP	missense variant	P/L	2549	1	0	889	possibly damaging	0.888	25001	likely benign	25
24583	MLL2	rs750113134	SNP	missense variant	P/S	2549	361	0.36	109	benign	0.108	19001	likely benign	19
24584	MLL2	rs575775792	SNP	missense variant	K/E	2548	91	0.09	122	benign	0.121	22001	likely benign	22
24585	MLL2	rs766114622	SNP	missense variant	S/F	2546	701	0.7	1	benign	0	16001	likely benign	16
24586	MLL2	rs766114622	SNP	missense variant	S/C	2546	171	0.17	157	benign	0.156	18001	likely benign	18
24587	MLL2	rs199742377	SNP	missense variant	P/A	2545	1	0	80	benign	0.079	20001	likely benign	20
24588	MLL2	rs764131120	SNP	missense variant	G/V	2543	31	0.03	947	probably damaging	0.946	23001	likely benign	23
24589	MLL2	rs993899550	SNP	missense variant	V/I	2542	91	0.09	38	benign	0.037	15001	likely benign	15
24590	MLL2	rs1380114567	SNP	missense variant	A/V	2541	111	0.11	6	benign	0.005	13001	likely benign	13

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