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
17151	FOXA1	rs767829889	SNP	missense variant	A/S	133	541	0.54	4	benign	0.003	15001	likely benign	15
17152	FOXA1	rs1341491551	SNP	missense variant	A/D	132	261	0.26	164	benign	0.163	21001	likely benign	21
17153	FOXA1	rs1449744866	SNP	missense variant	Y/C	130	1	0	996	probably damaging	0.995	28001	likely benign	28
17154	FOXA1	rs1566824631	SNP	missense variant	P/L	129	21	0.02	139	benign	0.138	23001	likely benign	23
17155	FOXA1	rs975102595	SNP	missense variant	L/R	127	1	0	987	probably damaging	0.986	27001	likely benign	27
17156	FOXA1	rs975102595	SNP	missense variant	L/P	127	1	0	991	probably damaging	0.99	27001	likely benign	27
17157	FOXA1	rs1228483575	SNP	missense variant	G/D	126	11	0.01	426	benign	0.425	23001	likely benign	23
17158	FOXA1	rs1326987182	SNP	missense variant	M/I	124	101	0.1	13	benign	0.012	22001	likely benign	22
17159	FOXA1	rs1326987182	SNP	missense variant	M/I	124	101	0.1	13	benign	0.012	22001	likely benign	22
17160	FOXA1	rs1208073239	SNP	missense variant	M/R	124	1	0	602	possibly damaging	0.601	27001	likely benign	27

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