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
22771	MLL2	rs1373629009	SNP	missense variant	E/A	5011	41	0.04	992	probably damaging	0.991	28001	likely benign	28
22772	MLL2	rs777295270	SNP	missense variant	E/Q	5011	31	0.03	995	probably damaging	0.994	26001	likely benign	26
22773	MLL2	rs746748048	SNP	missense variant	E/K	5008	71	0.07	238	benign	0.237	23001	likely benign	23
22774	MLL2	rs757097673	SNP	missense variant	R/Q	5007	91	0.09	792	possibly damaging	0.791	23001	likely benign	23
22775	MLL2	rs201855029	SNP	missense variant	R/W	5007	1	0	973	probably damaging	0.972	26001	likely benign	26
22776	MLL2	rs1335732588	SNP	missense variant	E/V	5006	1	0	725	possibly damaging	0.724	25001	likely benign	25
22777	MLL2	rs587778484	SNP	missense variant	E/V	5004	21	0.02	923	probably damaging	0.922	25001	likely benign	25
22778	MLL2	rs1376479615	SNP	missense variant	Q/R	5003	851	0.85	1	benign	0	15001	likely benign	15
22779	MLL2	rs745842900	SNP	missense variant	R/Q	5002	161	0.16	1	benign	0	16001	likely benign	16
22780	MLL2	rs768594066	SNP	missense variant	R/W	5002	1	0	250	benign	0.249	23001	likely benign	23

Left 2277 2278 2279