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
8791	KM2TC-MLL3	rs1235467493	SNP	missense variant	G/E	1817	1	0	1000	probably damaging	0.999	24001	likely benign	24
8792	KM2TC-MLL3	rs1278339836	SNP	missense variant	N/H	1816	1	0	727	possibly damaging	0.726	23001	likely benign	23
8793	KM2TC-MLL3	rs199626335	SNP	missense variant	G/V	1815	11	0.01	618	possibly damaging	0.617	23001	likely benign	23
8794	KM2TC-MLL3	rs753287348	SNP	missense variant	Q/L	1813	1	0	880	possibly damaging	0.879	26001	likely benign	26
8795	KM2TC-MLL3	rs753287348	SNP	missense variant	Q/R	1813	21	0.02	816	possibly damaging	0.815	25001	likely benign	25
8796	KM2TC-MLL3	rs778172326	SNP	missense variant	P/L	1812	1	0	358	benign	0.357	24001	likely benign	24
8797	KM2TC-MLL3	rs1252594627	SNP	missense variant	L/W	1810	31	0.03	999	probably damaging	0.998	25001	likely benign	25
8798	KM2TC-MLL3	rs1479368089	SNP	missense variant	P/H	1809	1	0	999	probably damaging	0.998	26001	likely benign	26
8799	KM2TC-MLL3	rs1354718519	SNP	missense variant	Q/H	1807	61	0.06	994	probably damaging	0.993	20001	likely benign	20
8800	KM2TC-MLL3	rs747374662	SNP	missense variant	I/T	1806	811	0.81	37	benign	0.036	14001	likely benign	14

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