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
11381	AKT1	rs1016707349	SNP	missense variant	A/T	171	191	0.19	12	benign	0.011	22001	likely benign	22
11382	AKT1	rs774284624	SNP	missense variant	K/N	170	21	0.02	345	benign	0.344	23001	likely benign	23
11383	AKT1	rs1183083759	SNP	missense variant	K/E	168	31	0.03	136	benign	0.135	24001	likely benign	24
11384	AKT1	rs11555433	SNP	missense variant	V/A	167	691	0.69	35	benign	0.034	21001	likely benign	21
11385	AKT1	rs1244026143	SNP	missense variant	V/G	164	11	0.01	980	probably damaging	0.979	31001	likely deleterious	31
11386	AKT1	rs1352687393	SNP	missense variant	K/M	163	1	0	971	probably damaging	0.97	28001	likely benign	28
11387	AKT1	rs980441042	SNP	missense variant	T/A	160	1	0	478	possibly damaging	0.477	26001	likely benign	26
11388	AKT1	rs866169013	SNP	missense variant	G/V	159	41	0.04	662	possibly damaging	0.661	26001	likely benign	26
11389	AKT1	rs568870136	SNP	missense variant	G/R	157	1	0	995	probably damaging	0.994	28001	likely benign	28
11390	AKT1	rs1277434432	SNP	missense variant	M/I	147	91	0.09	16	benign	0.015	22001	likely benign	22

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