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
16521	ESR1	rs1447425129	SNP	missense variant	A/T	66	371	0.37	6	benign	0.005	22001	likely benign	22
16522	ESR1	rs747623367	SNP	missense variant	A/S	67	221	0.22	163	benign	0.162	20001	likely benign	20
16523	ESR1	rs771540162	SNP	missense variant	A/T	68	421	0.42	214	benign	0.213	16001	likely benign	16
16524	ESR1	rs771540162	SNP	missense variant	A/S	68	381	0.38	903	possibly damaging	0.902	19001	likely benign	19
16525	ESR1	rs1301485751	SNP	missense variant	A/V	68	511	0.51	833	possibly damaging	0.832	21001	likely benign	21
16526	ESR1	rs1230497579	SNP	missense variant	N/D	69	181	0.18	1	benign	0	4001	likely benign	4
16527	ESR1	rs146586199	SNP	missense variant	N/K	69	251	0.25	2	benign	0.001	9001	likely benign	9
16528	ESR1	rs776480169	SNP	missense variant	A/G	70	361	0.36	765	possibly damaging	0.764	22001	likely benign	22
16529	ESR1	rs759317032	SNP	missense variant	Q/H	71	111	0.11	10	benign	0.009	8001	likely benign	8
16530	ESR1	rs769634976	SNP	missense variant	Y/C	73	11	0.01	976	probably damaging	0.975	27001	likely benign	27

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