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
12651	NCOR1	rs765835833	SNP	missense variant	L/F	56	11	0.01	983	probably damaging	0.982	27001	likely benign	27
12652	NCOR1	rs765835833	SNP	missense variant	L/V	56	131	0.13	875	possibly damaging	0.874	25001	likely benign	25
12653	NCOR1	rs576151037	SNP	missense variant	Q/H	55	911	0.91	83	benign	0.082	16001	likely benign	16
12654	NCOR1	rs1264306279	SNP	missense variant	A/V	53	91	0.09	767	possibly damaging	0.766	24001	likely benign	24
12655	NCOR1	rs970882438	SNP	missense variant	A/T	53	81	0.08	114	benign	0.113	19001	likely benign	19
12656	NCOR1	rs1301673402	SNP	missense variant	S/C	51	11	0.01	439	benign	0.438	22001	likely benign	22
12657	NCOR1	rs117442740	SNP	missense variant	V/M	50	151	0.15	946	probably damaging	0.945	23001	likely benign	23
12658	NCOR1	rs758568154	SNP	missense variant	L/V	48	111	0.11	14	benign	0.013	14001	likely benign	14
12659	NCOR1	rs779950557	SNP	missense variant	H/R	47	1	0	993	probably damaging	0.992	25001	likely benign	25
12660	NCOR1	rs747285406	SNP	missense variant	R/H	44	111	0.11	949	probably damaging	0.948	24001	likely benign	24

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