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
7151	KM2TC-MLL3	rs764256216	SNP	missense variant	P/L	3950	51	0.05	881	possibly damaging	0.88	25001	likely benign	25
7152	KM2TC-MLL3	rs764256216	SNP	missense variant	P/R	3950	1	0	963	probably damaging	0.962	25001	likely benign	25
7153	KM2TC-MLL3	rs1055248357	SNP	missense variant	Q/E	3948	161	0.16	40	benign	0.039	22001	likely benign	22
7154	KM2TC-MLL3	rs1264362310	SNP	missense variant	G/R	3943	31	0.03	989	probably damaging	0.988	27001	likely benign	27
7155	KM2TC-MLL3	rs185334684	SNP	missense variant	K/R	3940	171	0.17	40	benign	0.039	21001	likely benign	21
7156	KM2TC-MLL3	rs1303611028	SNP	missense variant	H/Q	3936	181	0.18	2	benign	0.001	1	likely benign	0
7157	KM2TC-MLL3	rs565261136	SNP	missense variant	H/L	3936	1	0	37	benign	0.036	23001	likely benign	23
7158	KM2TC-MLL3	rs565261136	SNP	missense variant	H/R	3936	1	0	37	benign	0.036	23001	likely benign	23
7159	KM2TC-MLL3	rs775922637	SNP	missense variant	V/A	3934	1001	1	16	benign	0.015	15001	likely benign	15
7160	KM2TC-MLL3	rs763201432	SNP	missense variant	V/M	3934	61	0.06	7	benign	0.006	20001	likely benign	20

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