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
23121	MLL2	rs752523300	SNP	missense variant	K/R	4523	1	0	995	probably damaging	0.994	26001	likely benign	26
23122	MLL2	rs752523300	SNP	missense variant	K/T	4523	1	0	998	probably damaging	0.997	26001	likely benign	26
23123	MLL2	rs935977103	SNP	missense variant	P/S	4522	181	0.18	35	benign	0.034	22001	likely benign	22
23124	MLL2	rs374531508	SNP	missense variant	P/L	4520	11	0.01	1	benign	0	23001	likely benign	23
23125	MLL2	rs1354376171	SNP	missense variant	P/S	4520	41	0.04	2	benign	0.001	21001	likely benign	21
23126	MLL2	rs891841128	SNP	missense variant	T/I	4519	131	0.13	4	benign	0.003	21001	likely benign	21
23127	MLL2	rs1290937992	SNP	missense variant	P/L	4517	1	0	53	benign	0.052	24001	likely benign	24
23128	MLL2	rs745951896	SNP	missense variant	P/A	4517	181	0.18	27	benign	0.026	21001	likely benign	21
23129	MLL2	rs780298528	SNP	missense variant	A/T	4513	451	0.45	237	benign	0.236	19001	likely benign	19
23130	MLL2	rs1190525652	SNP	missense variant	A/G	4512	391	0.39	11	benign	0.01	17001	likely benign	17

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