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
23171	MLL2	rs761717148	SNP	missense variant	R/G	4468	1	0	847	possibly damaging	0.846	27001	likely benign	27
23172	MLL2	rs1307252507	SNP	missense variant	L/V	4467	1	0	992	probably damaging	0.991	24001	likely benign	24
23173	MLL2	rs1283072905	SNP	missense variant	Q/E	4464	1	0	971	probably damaging	0.97	25001	likely benign	25
23174	MLL2	rs1283072905	SNP	missense variant	Q/K	4464	191	0.19	981	probably damaging	0.98	24001	likely benign	24
23175	MLL2	rs1476524664	SNP	missense variant	S/A	4456	11	0.01	50	benign	0.049	23001	likely benign	23
23176	MLL2	rs372839823	SNP	missense variant	R/L	4455	11	0.01	998	probably damaging	0.997	26001	likely benign	26
23177	MLL2	rs372839823	SNP	missense variant	R/H	4455	1	0	998	probably damaging	0.997	26001	likely benign	26
23178	MLL2	rs530054198	SNP	missense variant	R/C	4455	1	0	998	probably damaging	0.997	28001	likely benign	28
23179	MLL2	rs778075211	SNP	missense variant	P/R	4454	1	0	35	benign	0.034	22001	likely benign	22
23180	MLL2	rs1375999182	SNP	missense variant	G/D	4453	1	0	880	possibly damaging	0.879	24001	likely benign	24

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