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
14171	SPEN	rs560858640	SNP	missense variant	Q/H	1863	61	0.06	947	probably damaging	0.946	23001	likely benign	23
14172	SPEN	rs746458925	SNP	missense variant	K/Q	1864	1	0	992	probably damaging	0.991	26001	likely benign	26
14173	SPEN	rs746458925	SNP	missense variant	K/E	1864	1	0	981	probably damaging	0.98	26001	likely benign	26
14174	SPEN	rs954142908	SNP	missense variant	K/N	1864	1	0	992	probably damaging	0.991	24001	likely benign	24
14175	SPEN	rs1302081627	SNP	missense variant	L/S	1866	161	0.16	987	probably damaging	0.986	23001	likely benign	23
14176	SPEN	rs1395771400	SNP	missense variant	E/K	1867	1	0	908	possibly damaging	0.907	26001	likely benign	26
14177	SPEN	rs756861745	SNP	missense variant	A/V	1872	71	0.07	971	probably damaging	0.97	23001	likely benign	23
14178	SPEN	rs780679557	SNP	missense variant	I/F	1875	41	0.04	119	benign	0.118	22001	likely benign	22
14179	SPEN	rs769126178	SNP	missense variant	R/K	1877	121	0.12	816	possibly damaging	0.815	23001	likely benign	23
14180	SPEN	rs774918998	SNP	missense variant	K/E	1881	41	0.04	932	probably damaging	0.931	27001	likely benign	27

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