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
8571	KM2TC-MLL3	rs1477418525	SNP	missense variant	H/Y	2087	131	0.13	778	possibly damaging	0.777	23001	likely benign	23
8572	KM2TC-MLL3	rs1477418525	SNP	missense variant	H/D	2087	21	0.02	703	possibly damaging	0.702	25001	likely benign	25
8573	KM2TC-MLL3	rs773209299	SNP	missense variant	N/S	2084	721	0.72	2	benign	0.001	2001	likely benign	2
8574	KM2TC-MLL3	rs760480724	SNP	missense variant	I/T	2082	391	0.39	1	benign	0	8001	likely benign	8
8575	KM2TC-MLL3	rs765573319	SNP	missense variant	I/V	2082	1001	1	1	benign	0	1	likely benign	0
8576	KM2TC-MLL3	rs762977185	SNP	missense variant	R/G	2080	51	0.05	367	benign	0.366	22001	likely benign	22
8577	KM2TC-MLL3	rs1321521913	SNP	missense variant	P/L	2079	1	0	841	possibly damaging	0.84	26001	likely benign	26
8578	KM2TC-MLL3	rs1225336268	SNP	missense variant	P/L	2075	31	0.03	998	probably damaging	0.997	25001	likely benign	25
8579	KM2TC-MLL3	rs1035538964	SNP	missense variant	P/T	2075	1	0	998	probably damaging	0.997	25001	likely benign	25
8580	KM2TC-MLL3	rs781608784	SNP	missense variant	E/V	2073	11	0.01	997	probably damaging	0.996	26001	likely benign	26

Left 857 858 859