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
9021	KM2TC-MLL3	rs555704077	SNP	missense variant	P/T	1468	1	0	116	benign	0.115	20001	likely benign	20
9022	KM2TC-MLL3	rs1383716454	SNP	missense variant	T/A	1465	1001	1	1	benign	0	1	likely benign	0
9023	KM2TC-MLL3	rs766174573	SNP	missense variant	V/D	1464	1	0	48	benign	0.047	19001	likely benign	19
9024	KM2TC-MLL3	rs1254246915	SNP	missense variant	I/T	1461	21	0.02	123	benign	0.122	22001	likely benign	22
9025	KM2TC-MLL3	rs773738226	SNP	missense variant	H/R	1458	321	0.32	2	benign	0.001	16001	likely benign	16
9026	KM2TC-MLL3	rs1181024979	SNP	missense variant	D/G	1457	111	0.11	4	benign	0.003	21001	likely benign	21
9027	KM2TC-MLL3	rs1435221359	SNP	missense variant	V/I	1456	141	0.14	54	benign	0.053	21001	likely benign	21
9028	KM2TC-MLL3	rs747478461	SNP	missense variant	S/P	1455	161	0.16	13	benign	0.012	23001	likely benign	23
9029	KM2TC-MLL3	rs373427953	SNP	missense variant	A/S	1453	241	0.24	58	benign	0.057	20001	likely benign	20
9030	KM2TC-MLL3	rs566020227	SNP	missense variant	L/I	1452	31	0.03	979	probably damaging	0.978	23001	likely benign	23

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