Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
7731	KM2TC-MLL3	rs145072739	SNP	missense variant	R/C	3177	1	0	996	probably damaging	0.995	29001	likely benign	29
7732	KM2TC-MLL3	rs773038479	SNP	missense variant	D/N	3174	231	0.23	717	possibly damaging	0.716	24001	likely benign	24
7733	KM2TC-MLL3	rs200919055	SNP	missense variant	F/L	3171	1	0	971	probably damaging	0.97	28001	likely benign	28
7734	KM2TC-MLL3	rs778495651	SNP	missense variant	G/V	3168	61	0.06	1000	probably damaging	0.999	25001	likely benign	25
7735	KM2TC-MLL3	rs1349254658	SNP	missense variant	N/K	3166	1	0	995	probably damaging	0.994	26001	likely benign	26
7736	KM2TC-MLL3	rs752338525	SNP	missense variant	I/T	3159	31	0.03	213	benign	0.212	23001	likely benign	23
7737	KM2TC-MLL3	rs1277612900	SNP	missense variant	I/V	3155	191	0.19	7	benign	0.006	19001	likely benign	19
7738	KM2TC-MLL3	rs767049285	SNP	missense variant	P/S	3150	241	0.24	1	benign	0	1	likely benign	0
7739	KM2TC-MLL3	rs767049285	SNP	missense variant	P/T	3150	871	0.87	1	benign	0	1	likely benign	0
7740	KM2TC-MLL3	rs1026459564	SNP	missense variant	A/V	3148	391	0.39	7	benign	0.006	18001	likely benign	18

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