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
24481	MLL2	rs774371343	SNP	missense variant	Q/H	2665	1	0	957	probably damaging	0.956	23001	likely benign	23
24482	MLL2	rs895906051	SNP	missense variant	Q/R	2665	51	0.05	916	probably damaging	0.915	25001	likely benign	25
24483	MLL2	rs767751306	SNP	missense variant	T/S	2664	241	0.24	2	benign	0.001	11001	likely benign	11
24484	MLL2	rs1041690934	SNP	missense variant	G/D	2663	11	0.01	25	benign	0.024	19001	likely benign	19
24485	MLL2	rs1370465303	SNP	missense variant	L/F	2661	1	0	739	possibly damaging	0.738	23001	likely benign	23
24486	MLL2	rs200913080	SNP	missense variant	A/V	2657	331	0.33	1	benign	0	9001	likely benign	9
24487	MLL2	rs1014845953	SNP	missense variant	L/S	2656	171	0.17	101	benign	0.1	22001	likely benign	22
24488	MLL2	rs1226177022	SNP	missense variant	S/C	2655	1	0	819	possibly damaging	0.818	25001	likely benign	25
24489	MLL2	rs766926297	SNP	missense variant	S/P	2655	141	0.14	8	benign	0.007	22001	likely benign	22
24490	MLL2	rs766926297	SNP	missense variant	S/T	2655	131	0.13	24	benign	0.023	21001	likely benign	21

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