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
9241	KM2TC-MLL3	rs1292944471	SNP	missense variant	M/I	1135	131	0.13	4	benign	0.003	20001	likely benign	20
9242	KM2TC-MLL3	rs778507711	SNP	missense variant	M/V	1135	31	0.03	15	benign	0.014	20001	likely benign	20
9243	KM2TC-MLL3	rs4024339	SNP	missense variant	S/N	1134	61	0.06	277	benign	0.276	22001	likely benign	22
9244	KM2TC-MLL3	rs752352968	SNP	missense variant	G/A	1130	1	0	944	probably damaging	0.943	24001	likely benign	24
9245	KM2TC-MLL3	rs757867244	SNP	missense variant	I/T	1129	641	0.64	2	benign	0.001	18001	likely benign	18
9246	KM2TC-MLL3	rs777278245	SNP	missense variant	I/F	1129	251	0.25	70	benign	0.069	19001	likely benign	19
9247	KM2TC-MLL3	rs1298652424	SNP	missense variant	A/S	1127	31	0.03	995	probably damaging	0.994	24001	likely benign	24
9248	KM2TC-MLL3	rs1395745039	SNP	missense variant	N/D	1125	171	0.17	116	benign	0.115	20001	likely benign	20
9249	KM2TC-MLL3	rs1270510831	SNP	missense variant	E/D	1124	1	0	992	probably damaging	0.991	23001	likely benign	23
9250	KM2TC-MLL3	rs1019340795	SNP	missense variant	V/L	1123	21	0.02	988	probably damaging	0.987	24001	likely benign	24

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