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
6971	KM2TC-MLL3	rs1339162677	SNP	missense variant	K/E	4222	311	0.31	36	benign	0.035	20001	likely benign	20
6972	KM2TC-MLL3	rs1201348614	SNP	missense variant	N/S	4221	591	0.59	1	benign	0	5001	likely benign	5
6973	KM2TC-MLL3	rs139111507	SNP	missense variant	L/V	4219	381	0.38	27	benign	0.026	9001	likely benign	9
6974	KM2TC-MLL3	rs139111507	SNP	missense variant	L/I	4219	211	0.21	7	benign	0.006	11001	likely benign	11
6975	KM2TC-MLL3	rs200004824	SNP	missense variant	L/M	4217	11	0.01	279	benign	0.278	21001	likely benign	21
6976	KM2TC-MLL3	rs756572043	SNP	missense variant	K/E	4215	11	0.01	59	benign	0.058	22001	likely benign	22
6977	KM2TC-MLL3	rs780271402	SNP	missense variant	R/Q	4211	231	0.23	947	probably damaging	0.946	25001	likely benign	25
6978	KM2TC-MLL3	rs367652375	SNP	missense variant	R/W	4211	21	0.02	984	probably damaging	0.983	26001	likely benign	26
6979	KM2TC-MLL3	rs768150468	SNP	missense variant	G/R	4209	1	0	999	probably damaging	0.998	26001	likely benign	26
6980	KM2TC-MLL3	rs1352976610	SNP	missense variant	S/R	4208	21	0.02	803	possibly damaging	0.802	24001	likely benign	24

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