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
24291	MLL2	rs988820724	SNP	missense variant	G/C	2923	11	0.01	629	possibly damaging	0.628	23001	likely benign	23
24292	MLL2	rs757791539	SNP	missense variant	R/Q	2922	291	0.29	49	benign	0.048	21001	likely benign	21
24293	MLL2	rs751964761	SNP	missense variant	R/W	2922	1	0	929	probably damaging	0.928	27001	likely benign	27
24294	MLL2	rs751133364	SNP	missense variant	L/H	2921	41	0.04	748	possibly damaging	0.747	25001	likely benign	25
24295	MLL2	rs1485781380	SNP	missense variant	P/L	2918	1	0	1	benign	0	23001	likely benign	23
24296	MLL2	rs781113013	SNP	missense variant	L/P	2916	101	0.1	2	benign	0.001	21001	likely benign	21
24297	MLL2	rs1420789348	SNP	missense variant	H/R	2914	281	0.28	16	benign	0.015	19001	likely benign	19
24298	MLL2	rs1386859726	SNP	missense variant	H/Y	2914	371	0.37	470	possibly damaging	0.469	22001	likely benign	22
24299	MLL2	rs1307203751	SNP	missense variant	P/S	2913	491	0.49	1	benign	0	10001	likely benign	10
24300	MLL2	rs757759802	SNP	missense variant	D/V	2912	61	0.06	4	benign	0.003	20001	likely benign	20

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