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
161	TP53	rs193920774	SNP	missense variant	G/V	266	1	0	982	probably damaging	0.981	29001	likely benign	29
162	TP53	rs193920774	SNP	missense variant	G/E	266	1	0	864	possibly damaging	0.863	28001	likely benign	28
163	TP53	rs1057519990	SNP	missense variant	G/R	266	21	0.02	774	possibly damaging	0.773	29001	likely benign	29
164	TP53	rs1057519990	SNP	missense variant	G/R	266	21	0.02	774	possibly damaging	0.773	29001	likely benign	29
165	TP53	rs879253942	SNP	missense variant	L/P	265	1	0	999	probably damaging	0.998	32001	likely deleterious	32
166	TP53	rs1555525353	SNP	missense variant	L/P	264	101	0.1	150	benign	0.149	23001	likely benign	23
167	TP53	rs770598448	SNP	missense variant	N/K	263	331	0.33	6	benign	0.005	1	likely benign	0
168	TP53	rs72661119	SNP	missense variant	N/D	263	231	0.23	7	benign	0.006	21001	likely benign	21
169	TP53	rs72661119	SNP	missense variant	N/H	263	131	0.13	22	benign	0.021	21001	likely benign	21
170	TP53	rs1131691025	SNP	missense variant	G/V	262	1	0	978	probably damaging	0.977	26001	likely benign	26

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