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
16331	PIK3R1	rs757124592	SNP	missense variant	D/G	67	1	0	737	possibly damaging	0.736	28001	likely benign	28
16332	PIK3R1	rs1202121850	SNP	missense variant	P/S	68	1	0	1000	probably damaging	0.999	25001	likely benign	25
16333	PIK3R1	rs1184230510	SNP	missense variant	V/A	74	1	0	998	probably damaging	0.997	27001	likely benign	27
16334	PIK3R1	rs779658023	SNP	missense variant	V/I	75	171	0.17	985	probably damaging	0.984	23001	likely benign	23
16335	PIK3R1	rs906052199	SNP	missense variant	V/A	75	21	0.02	999	probably damaging	0.998	27001	likely benign	27
16336	PIK3R1	rs1175989621	SNP	missense variant	R/W	82	1	0	890	possibly damaging	0.889	25001	likely benign	25
16337	PIK3R1	rs748784250	SNP	missense variant	R/Q	82	351	0.35	10	benign	0.009	23001	likely benign	23
16338	PIK3R1	rs1001616209	SNP	missense variant	L/I	98	21	0.02	26	benign	0.025	23001	likely benign	23
16339	PIK3R1	rs1001616209	SNP	missense variant	L/F	98	11	0.01	2	benign	0.001	23001	likely benign	23
16340	PIK3R1	rs768309285	SNP	missense variant	V/I	101	251	0.25	6	benign	0.005	22001	likely benign	22

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