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
7081	KM2TC-MLL3	rs774713295	SNP	missense variant	P/L	4070	121	0.12	11	benign	0.01	22001	likely benign	22
7082	KM2TC-MLL3	rs535432925	SNP	missense variant	G/V	4069	31	0.03	321	benign	0.32	23001	likely benign	23
7083	KM2TC-MLL3	rs535432925	SNP	missense variant	G/A	4069	11	0.01	353	benign	0.352	23001	likely benign	23
7084	KM2TC-MLL3	rs141966811	SNP	missense variant	A/V	4065	21	0.02	18	benign	0.017	23001	likely benign	23
7085	KM2TC-MLL3	rs1431921523	SNP	missense variant	Y/S	4063	41	0.04	27	benign	0.026	23001	likely benign	23
7086	KM2TC-MLL3	rs377630495	SNP	missense variant	Y/H	4063	51	0.05	124	benign	0.123	24001	likely benign	24
7087	KM2TC-MLL3	rs960292962	SNP	missense variant	T/A	4061	321	0.32	4	benign	0.003	16001	likely benign	16
7088	KM2TC-MLL3	rs1563166026	SNP	missense variant	G/S	4060	451	0.45	233	benign	0.232	19001	likely benign	19
7089	KM2TC-MLL3	rs565676457	SNP	missense variant	P/S	4059	1	0	933	probably damaging	0.932	25001	likely benign	25
7090	KM2TC-MLL3	rs754876682	SNP	missense variant	E/G	4058	1	0	881	possibly damaging	0.88	28001	likely benign	28

Left 708 709 710