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
26951	RUNX1	rs200431130	SNP	missense variant	M/K	25	1	0	922	probably damaging	0.921	29001	likely benign	29
26952	RUNX1	rs780977528	SNP	missense variant	K/N	24	11	0.01	992	probably damaging	0.991	28001	likely benign	28
26953	RUNX1	rs752298116	SNP	missense variant	P/L	22	41	0.04	151	benign	0.15	28001	likely benign	28
26954	RUNX1	rs755793721	SNP	missense variant	P/A	22	471	0.47	36	benign	0.035	20001	likely benign	20
26955	RUNX1	rs755793721	SNP	missense variant	P/T	22	181	0.18	58	benign	0.057	22001	likely benign	22
26956	RUNX1	rs748720882	SNP	missense variant	S/N	21	91	0.09	969	probably damaging	0.968	24001	likely benign	24
26957	RUNX1	rs770530237	SNP	missense variant	L/P	20	31	0.03	998	probably damaging	0.997	32001	likely deleterious	32
26958	RUNX1	rs770530237	SNP	missense variant	L/Q	20	1	0	998	probably damaging	0.997	32001	likely deleterious	32
26959	RUNX1	rs1555899881	SNP	missense variant	P/S	16	1	0	997	probably damaging	0.996	29001	likely benign	29
26960	RUNX1	rs769087155	SNP	missense variant	T/M	14	1	0	997	probably damaging	0.996	31001	likely deleterious	31

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