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
17871	AKT2	rs1380555769	SNP	missense variant	Q/R	71	41	0.04	56	benign	0.055	24001	likely benign	24
17872	AKT2	rs777417874	SNP	missense variant	A/P	68	181	0.18	903	possibly damaging	0.902	2001	likely benign	2
17873	AKT2	rs770748153	SNP	missense variant	L/P	63	201	0.2	1	unknown	0	3001	likely benign	3
17874	AKT2	rs774226881	SNP	missense variant	P/S	60	1001	1	1	unknown	0	5001	likely benign	5
17875	AKT2	rs774226881	SNP	missense variant	P/A	60	441	0.44	1	unknown	0	3001	likely benign	3
17876	AKT2	rs745845373	SNP	missense variant	A/V	59	211	0.21	1	unknown	0	7001	likely benign	7
17877	AKT2	rs1407888862	SNP	missense variant	V/I	57	191	0.19	147	benign	0.146	22001	likely benign	22
17878	AKT2	rs770250877	SNP	missense variant	P/L	51	61	0.06	887	possibly damaging	0.886	28001	likely benign	28
17879	AKT2	rs770250877	SNP	missense variant	P/R	51	11	0.01	887	possibly damaging	0.886	28001	likely benign	28
17880	AKT2	rs201145928	SNP	missense variant	P/A	51	41	0.04	30	benign	0.029	24001	likely benign	24

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