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
26781	RUNX1	rs759227406	SNP	missense variant	P/Q	251	31	0.03	882	possibly damaging	0.881	26001	likely benign	26
26782	RUNX1	rs767251526	SNP	missense variant	P/S	251	311	0.31	40	benign	0.039	21001	likely benign	21
26783	RUNX1	rs1397817592	SNP	missense variant	S/A	249	71	0.07	932	probably damaging	0.931	26001	likely benign	26
26784	RUNX1	rs201164283	SNP	missense variant	P/L	248	21	0.02	26	benign	0.025	24001	likely benign	24
26785	RUNX1	rs370766377	SNP	missense variant	Q/H	247	21	0.02	980	probably damaging	0.979	24001	likely benign	24
26786	RUNX1	rs556287817	SNP	missense variant	Q/R	247	91	0.09	933	probably damaging	0.932	24001	likely benign	24
26787	RUNX1	rs750826029	SNP	missense variant	R/K	244	51	0.05	1	benign	0	22001	likely benign	22
26788	RUNX1	rs1060502574	SNP	missense variant	D/H	242	11	0.01	991	probably damaging	0.99	27001	likely benign	27
26789	RUNX1	rs757570529	SNP	missense variant	M/I	240	1001	1	1	benign	0	14001	likely benign	14
26790	RUNX1	rs765362075	SNP	missense variant	Q/E	237	41	0.04	32	benign	0.031	23001	likely benign	23

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