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
24101	MLL2	rs919478619	SNP	missense variant	G/V	3189	131	0.13	123	benign	0.122	17001	likely benign	17
24102	MLL2	rs774803178	SNP	missense variant	G/R	3189	61	0.06	23	benign	0.022	20001	likely benign	20
24103	MLL2	rs774803178	SNP	missense variant	G/R	3189	61	0.06	23	benign	0.022	20001	likely benign	20
24104	MLL2	rs762206028	SNP	missense variant	T/M	3188	1	0	960	probably damaging	0.959	24001	likely benign	24
24105	MLL2	rs762206028	SNP	missense variant	T/R	3188	51	0.05	969	probably damaging	0.968	23001	likely benign	23
24106	MLL2	rs768113078	SNP	missense variant	T/A	3188	131	0.13	438	benign	0.437	18001	likely benign	18
24107	MLL2	rs1435084589	SNP	missense variant	A/V	3187	51	0.05	15	benign	0.014	21001	likely benign	21
24108	MLL2	rs760323567	SNP	missense variant	A/S	3187	141	0.14	1	benign	0	9001	likely benign	9
24109	MLL2	rs766004779	SNP	missense variant	G/E	3186	41	0.04	880	possibly damaging	0.879	23001	likely benign	23
24110	MLL2	rs753471362	SNP	missense variant	G/R	3186	21	0.02	943	probably damaging	0.942	24001	likely benign	24

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