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
27851	XBP1	rs1441327428	SNP	missense variant	A/T	28	691	0.69	1	benign	0	21001	likely benign	21
27852	XBP1	rs1214878879	SNP	missense variant	A/T	27	301	0.3	1	benign	0	16001	likely benign	16
27853	XBP1	rs1282596667	SNP	missense variant	A/T	25	101	0.1	178	benign	0.177	18001	likely benign	18
27854	XBP1	rs1223883748	SNP	missense variant	P/A	24	711	0.71	8	benign	0.007	9001	likely benign	9
27855	XBP1	rs1356385471	SNP	missense variant	Q/R	23	81	0.08	1	benign	0	18001	likely benign	18
27856	XBP1	rs548654399	SNP	missense variant	G/E	22	1	0	657	possibly damaging	0.656	23001	likely benign	23
27857	XBP1	rs1197052678	SNP	missense variant	L/P	19	1	0	1000	probably damaging	0.999	25001	likely benign	25
27858	XBP1	rs774935023	SNP	missense variant	L/F	19	91	0.09	999	probably damaging	0.998	23001	likely benign	23
27859	XBP1	rs570172086	SNP	missense variant	P/L	15	131	0.13	454	possibly damaging	0.453	21001	likely benign	21
27860	XBP1	rs957598990	SNP	missense variant	P/S	15	211	0.21	22	benign	0.021	18001	likely benign	18

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