Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
27251	USP9X	rs1376493241	SNP	missense variant	A/S	1097	601	0.6	19	benign	0.018	20001	likely benign	20
27252	USP9X	rs1555927212	SNP	missense variant	A/T	1102	1	0	906	possibly damaging	0.905	27001	likely benign	27
27253	USP9X	rs1370040222	SNP	missense variant	P/S	1105	61	0.06	8	benign	0.007	21001	likely benign	21
27254	USP9X	rs778641876	SNP	missense variant	P/L	1105	1	0	101	benign	0.1	23001	likely benign	23
27255	USP9X	rs1257518889	SNP	missense variant	A/G	1107	531	0.53	1	benign	0	19001	likely benign	19
27256	USP9X	rs776528655	SNP	missense variant	H/R	1116	41	0.04	10	benign	0.009	23001	likely benign	23
27257	USP9X	rs752427844	SNP	missense variant	L/M	1127	91	0.09	629	possibly damaging	0.628	19001	likely benign	19
27258	USP9X	rs1274391019	SNP	missense variant	S/C	1128	21	0.02	631	possibly damaging	0.63	25001	likely benign	25
27259	USP9X	rs765495325	SNP	missense variant	S/N	1128	711	0.71	4	benign	0.003	19001	likely benign	19
27260	USP9X	rs868523294	SNP	missense variant	F/L	1135	41	0.04	887	possibly damaging	0.886	23001	likely benign	23

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