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
22591	MLL2	rs1459471282	SNP	missense variant	T/M	5297	1	0	1001	probably damaging	1	28001	likely benign	28
22592	MLL2	rs1365163460	SNP	missense variant	E/D	5292	1001	1	472	possibly damaging	0.471	18001	likely benign	18
22593	MLL2	rs771191137	SNP	missense variant	E/D	5291	11	0.01	999	probably damaging	0.998	23001	likely benign	23
22594	MLL2	rs936142615	SNP	missense variant	E/K	5291	1	0	1000	probably damaging	0.999	29001	likely benign	29
22595	MLL2	rs746132916	SNP	missense variant	L/R	5288	1	0	986	probably damaging	0.985	29001	likely benign	29
22596	MLL2	rs1390758510	SNP	missense variant	Y/C	5287	1	0	991	probably damaging	0.99	29001	likely benign	29
22597	MLL2	rs1555185337	SNP	missense variant	P/R	5285	1	0	968	probably damaging	0.967	33001	likely deleterious	33
22598	MLL2	rs376465820	SNP	missense variant	R/Q	5282	681	0.68	955	probably damaging	0.954	23001	likely benign	23
22599	MLL2	rs769137344	SNP	missense variant	A/T	5278	241	0.24	427	benign	0.426	22001	likely benign	22
22600	MLL2	rs1301874523	SNP	missense variant	K/R	5276	181	0.18	32	benign	0.031	22001	likely benign	22

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