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
7471	KM2TC-MLL3	rs760204735	SNP	missense variant	L/I	3539	291	0.29	16	benign	0.015	15001	likely benign	15
7472	KM2TC-MLL3	rs375465800	SNP	missense variant	H/Y	3536	21	0.02	198	benign	0.197	22001	likely benign	22
7473	KM2TC-MLL3	rs1409570941	SNP	missense variant	K/N	3533	21	0.02	987	probably damaging	0.986	23001	likely benign	23
7474	KM2TC-MLL3	rs764946605	SNP	missense variant	V/L	3532	71	0.07	15	benign	0.014	8001	likely benign	8
7475	KM2TC-MLL3	rs11541588	SNP	missense variant	S/C	3530	51	0.05	175	benign	0.174	12001	likely benign	12
7476	KM2TC-MLL3	rs373378915	SNP	missense variant	N/Y	3528	1	0	260	benign	0.259	21001	likely benign	21
7477	KM2TC-MLL3	rs373378915	SNP	missense variant	N/D	3528	51	0.05	25	benign	0.024	17001	likely benign	17
7478	KM2TC-MLL3	rs761972117	SNP	missense variant	G/R	3525	11	0.01	997	probably damaging	0.996	24001	likely benign	24
7479	KM2TC-MLL3	rs143821095	SNP	missense variant	P/L	3523	1	0	2	benign	0.001	23001	likely benign	23
7480	KM2TC-MLL3	rs750508218	SNP	missense variant	I/M	3522	121	0.12	101	benign	0.1	6001	likely benign	6

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