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
30651	AXIN1	rs1294561903	SNP	missense variant	Q/R	4	651	0.65	118	benign	0.117	17001	likely benign	17
30652	BCOR	rs778509180	SNP	missense variant	S/R	26	1	0	83	benign	0.082	23001	likely benign	23
30653	BCOR	rs757971608	SNP	missense variant	A/V	25	21	0.02	4	benign	0.003	24001	likely benign	24
30654	BCOR	rs779804763	SNP	missense variant	A/T	25	141	0.14	1	benign	0	16001	likely benign	16
30655	BCOR	rs947946150	SNP	missense variant	M/I	22	1	0	115	benign	0.114	22001	likely benign	22
30656	BCOR	rs748428774	SNP	missense variant	M/T	22	1	0	201	benign	0.2	23001	likely benign	23
30657	BCOR	rs377693413	SNP	missense variant	M/L	22	1	0	4	benign	0.003	22001	likely benign	22
30658	BCOR	rs778129253	SNP	missense variant	R/H	21	1	0	859	possibly damaging	0.858	26001	likely benign	26
30659	BCOR	rs749734466	SNP	missense variant	E/G	18	1	0	827	possibly damaging	0.826	27001	likely benign	27
30660	BCOR	rs771428828	SNP	missense variant	S/R	17	1	0	199	benign	0.198	23001	likely benign	23

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