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
29131	ATR	rs1242953145	SNP	missense variant	N/S	374	711	0.71	1	benign	0	8001	likely benign	8
29132	ATR	rs767456923	SNP	missense variant	V/D	370	611	0.61	37	benign	0.036	7001	likely benign	7
29133	ATR	rs773257754	SNP	missense variant	V/I	370	191	0.19	1	benign	0	13001	likely benign	13
29134	ATR	rs1461321227	SNP	missense variant	K/R	369	531	0.53	7	benign	0.006	20001	likely benign	20
29135	ATR	rs1254653974	SNP	missense variant	R/S	368	1	0	992	probably damaging	0.991	22001	likely benign	22
29136	ATR	rs751784387	SNP	missense variant	G/E	360	181	0.18	8	benign	0.007	19001	likely benign	19
29137	ATR	rs1422398912	SNP	missense variant	G/R	360	21	0.02	236	benign	0.235	24001	likely benign	24
29138	ATR	rs866710163	SNP	missense variant	P/S	358	21	0.02	470	possibly damaging	0.469	25001	likely benign	25
29139	ATR	rs1207025746	SNP	missense variant	V/E	357	21	0.02	470	possibly damaging	0.469	25001	likely benign	25
29140	ATR	rs759811121	SNP	missense variant	V/L	357	31	0.03	528	possibly damaging	0.527	24001	likely benign	24

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