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
26691	RUNX1	rs867474432	SNP	missense variant	G/D	340	11	0.01	204	benign	0.203	25001	likely benign	25
26692	RUNX1	rs1225645057	SNP	missense variant	G/V	338	1	0	61	benign	0.06	25001	likely benign	25
26693	RUNX1	rs752616540	SNP	missense variant	G/C	338	1	0	688	possibly damaging	0.687	27001	likely benign	27
26694	RUNX1	rs752616540	SNP	missense variant	G/R	338	1	0	347	benign	0.346	27001	likely benign	27
26695	RUNX1	rs752616540	SNP	missense variant	G/S	338	781	0.78	44	benign	0.043	23001	likely benign	23
26696	RUNX1	rs777498866	SNP	missense variant	G/A	336	131	0.13	76	benign	0.075	17001	likely benign	17
26697	RUNX1	rs1456340235	SNP	missense variant	S/L	335	81	0.08	256	benign	0.255	23001	likely benign	23
26698	RUNX1	rs1017287894	SNP	missense variant	T/I	334	11	0.01	331	benign	0.33	25001	likely benign	25
26699	RUNX1	rs1017287894	SNP	missense variant	T/S	334	401	0.4	7	benign	0.006	21001	likely benign	21
26700	RUNX1	rs778511514	SNP	missense variant	V/A	333	31	0.03	957	probably damaging	0.956	24001	likely benign	24

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