Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
19301	SETD2	rs6767907	SNP	missense variant	N/K	1027	71	0.07	72	benign	0.071	18001	likely benign	18
19302	SETD2	rs777213195	SNP	missense variant	D/G	1026	21	0.02	687	possibly damaging	0.686	23001	likely benign	23
19303	SETD2	rs1417600727	SNP	missense variant	I/M	1025	461	0.46	10	benign	0.009	13001	likely benign	13
19304	SETD2	rs200491606	SNP	missense variant	I/R	1025	291	0.29	302	benign	0.301	19001	likely benign	19
19305	SETD2	rs200491606	SNP	missense variant	I/T	1025	611	0.61	6	benign	0.005	13001	likely benign	13
19306	SETD2	rs757222335	SNP	missense variant	S/N	1021	181	0.18	25	benign	0.024	9001	likely benign	9
19307	SETD2	rs141227139	SNP	missense variant	S/F	1020	731	0.73	2	benign	0.001	14001	likely benign	14
19308	SETD2	rs115323681	SNP	missense variant	Q/R	1019	81	0.08	576	possibly damaging	0.575	21001	likely benign	21
19309	SETD2	rs1191319440	SNP	missense variant	T/I	1018	141	0.14	8	benign	0.007	15001	likely benign	15
19310	SETD2	rs771866928	SNP	missense variant	S/F	1016	1	0	938	probably damaging	0.937	22001	likely benign	22

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