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
22621	MLL2	rs1382079160	SNP	missense variant	L/R	5253	1	0	793	possibly damaging	0.792	28001	likely benign	28
22622	MLL2	rs1293861686	SNP	missense variant	G/V	5249	1	0	971	probably damaging	0.97	26001	likely benign	26
22623	MLL2	rs1293861686	SNP	missense variant	G/D	5249	11	0.01	990	probably damaging	0.989	26001	likely benign	26
22624	MLL2	rs1213973719	SNP	missense variant	G/S	5249	31	0.03	957	probably damaging	0.956	26001	likely benign	26
22625	MLL2	rs1326023273	SNP	missense variant	Q/H	5248	191	0.19	101	benign	0.1	18001	likely benign	18
22626	MLL2	rs887773024	SNP	missense variant	I/V	5246	791	0.79	4	benign	0.003	15001	likely benign	15
22627	MLL2	rs1321544261	SNP	missense variant	K/R	5244	1001	1	8	benign	0.007	17001	likely benign	17
22628	MLL2	rs1242959077	SNP	missense variant	V/L	5242	131	0.13	4	benign	0.003	4001	likely benign	4
22629	MLL2	rs374725382	SNP	missense variant	P/L	5239	1	0	1000	probably damaging	0.999	29001	likely benign	29
22630	MLL2	rs1480603091	SNP	missense variant	R/Q	5238	111	0.11	764	possibly damaging	0.763	24001	likely benign	24

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