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
16541	ESR1	rs1397883286	SNP	missense variant	P/H	79	101	0.1	326	benign	0.325	14001	likely benign	14
16542	ESR1	rs750873681	SNP	missense variant	Y/D	80	71	0.07	1000	probably damaging	0.999	24001	likely benign	24
16543	ESR1	rs572261788	SNP	missense variant	Y/C	80	41	0.04	1001	probably damaging	1	25001	likely benign	25
16544	ESR1	rs756487587	SNP	missense variant	G/S	81	181	0.18	184	benign	0.183	22001	likely benign	22
16545	ESR1	rs766797889	SNP	missense variant	G/V	81	81	0.08	244	benign	0.243	22001	likely benign	22
16546	ESR1	rs1340533809	SNP	missense variant	P/T	82	41	0.04	11	benign	0.01	21001	likely benign	21
16547	ESR1	rs1256665087	SNP	missense variant	G/E	83	161	0.16	244	benign	0.243	22001	likely benign	22
16548	ESR1	rs1307404491	SNP	missense variant	A/V	86	141	0.14	990	probably damaging	0.989	23001	likely benign	23
16549	ESR1	rs1267605861	SNP	missense variant	A/V	87	281	0.28	98	benign	0.097	20001	likely benign	20
16550	ESR1	rs956938848	SNP	missense variant	A/P	88	251	0.25	546	possibly damaging	0.545	23001	likely benign	23

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