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
29921	ATM	rs587782239	SNP	missense variant	C/F	44	11	0.01	86	benign	0.085	22001	likely benign	22
29922	ATM	rs762304746	SNP	missense variant	R/Q	46	91	0.09	853	possibly damaging	0.852	18001	likely benign	18
29923	ATM	rs762304746	SNP	missense variant	R/P	46	1	0	977	probably damaging	0.976	22001	likely benign	22
29924	ATM	rs1060501567	SNP	missense variant	H/Y	47	531	0.53	12	benign	0.011	12001	likely benign	12
29925	ATM	rs967371351	SNP	missense variant	H/R	47	201	0.2	284	benign	0.283	15001	likely benign	15
29926	ATM	rs1237700879	SNP	missense variant	H/Q	47	251	0.25	21	benign	0.02	1	likely benign	0
29927	ATM	rs202028401	SNP	missense variant	F/Y	48	1001	1	301	benign	0.3	5001	likely benign	5
29928	ATM	rs202028401	SNP	missense variant	F/S	48	581	0.58	7	benign	0.006	11001	likely benign	11
29929	ATM	rs202028401	SNP	missense variant	F/C	48	181	0.18	8	benign	0.007	12001	likely benign	12
29930	ATM	rs751327903	SNP	missense variant	F/L	48	741	0.74	4	benign	0.003	5001	likely benign	5

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