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
701	TP53	rs201753350	SNP	missense variant	V/F	31	161	0.16	23	benign	0.022	12001	likely benign	12
702	TP53	rs201753350	SNP	missense variant	V/I	31	261	0.26	6	benign	0.005	8001	likely benign	8
703	TP53	rs1011445550	SNP	missense variant	N/K	29	771	0.77	2	benign	0.001	8001	likely benign	8
704	TP53	rs786202289	SNP	missense variant	E/V	28	201	0.2	288	benign	0.287	22001	likely benign	22
705	TP53	rs1555526933	SNP	missense variant	P/L	27	81	0.08	161	benign	0.16	23001	likely benign	23
706	TP53	rs922736614	SNP	missense variant	P/S	27	111	0.11	273	benign	0.272	23001	likely benign	23
707	TP53	rs922736614	SNP	missense variant	P/T	27	151	0.15	250	benign	0.249	25001	likely benign	25
708	TP53	rs1800369	SNP	missense variant	D/E	21	531	0.53	18	benign	0.017	13001	likely benign	13
709	TP53	rs876659913	SNP	missense variant	S/P	20	111	0.11	133	benign	0.132	22001	likely benign	22
710	TP53	rs1567558112	SNP	missense variant	L/V	14	51	0.05	768	possibly damaging	0.767	23001	likely benign	23

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