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
1431	PTEN	rs587780007	SNP	missense variant	S/N	114	201	0.2	20	benign	0.019	22001	likely benign	22
1432	PTEN	rs587780007	SNP	missense variant	S/I	114	21	0.02	137	benign	0.136	24001	likely benign	24
1433	PTEN	rs876658345	SNP	missense variant	S/R	114	111	0.11	20	benign	0.019	21001	likely benign	21
1434	PTEN	rs786203858	SNP	missense variant	I/V	115	591	0.59	1	benign	0	19001	likely benign	19
1435	PTEN	rs746930141	SNP	missense variant	E/Q	116	391	0.39	50	benign	0.049	22001	likely benign	22
1436	PTEN	rs1197734477	SNP	missense variant	E/G	116	301	0.3	13	benign	0.012	22001	likely benign	22
1437	PTEN	rs1064794436	SNP	missense variant	R/C	117	121	0.12	6	benign	0.005	23001	likely benign	23
1438	PTEN	rs786201507	SNP	missense variant	R/H	117	161	0.16	6	benign	0.005	23001	likely benign	23
1439	PTEN	rs1564568473	SNP	missense variant	D/G	119	111	0.11	31	benign	0.03	24001	likely benign	24
1440	PTEN	rs878853946	SNP	missense variant	D/N	121	131	0.13	895	possibly damaging	0.894	23001	likely benign	23

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