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
931	MYC	rs1469075079	SNP	missense variant	T/I	188	241	0.24	133	benign	0.132	24001	likely benign	24
932	MYC	rs759774541	SNP	missense variant	S/Y	189	221	0.22	360	benign	0.359	24001	likely benign	24
933	MYC	rs1273381542	SNP	missense variant	L/S	191	761	0.76	79	benign	0.078	23001	likely benign	23
934	MYC	rs1273381542	SNP	missense variant	L/W	191	21	0.02	981	probably damaging	0.98	26001	likely benign	26
935	MYC	rs775690959	SNP	missense variant	Q/P	194	81	0.08	121	benign	0.12	25001	likely benign	25
936	MYC	rs775690959	SNP	missense variant	Q/R	194	201	0.2	884	possibly damaging	0.883	25001	likely benign	25
937	MYC	rs1474679499	SNP	missense variant	A/T	200	41	0.04	330	benign	0.329	25001	likely benign	25
938	MYC	rs1425055091	SNP	missense variant	E/K	202	11	0.01	921	probably damaging	0.92	29001	likely benign	29
939	MYC	rs1467496891	SNP	missense variant	C/Y	203	1	0	1000	probably damaging	0.999	32001	likely deleterious	32
940	MYC	rs1174781741	SNP	missense variant	I/T	204	1	0	969	probably damaging	0.968	32001	likely deleterious	32

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