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
19971	SETD2	rs1480415679	SNP	missense variant	S/F	132	141	0.14	161	benign	0.16	22001	likely benign	22
19972	SETD2	rs750623264	SNP	missense variant	I/V	131	1001	1	2	benign	0.001	3001	likely benign	3
19973	SETD2	rs1378977369	SNP	missense variant	T/I	130	591	0.59	6	benign	0.005	6001	likely benign	6
19974	SETD2	rs1308113254	SNP	missense variant	T/A	130	1001	1	6	benign	0.005	1	likely benign	0
19975	SETD2	rs1229892824	SNP	missense variant	Q/R	128	51	0.05	31	benign	0.03	18001	likely benign	18
19976	SETD2	rs1559749871	SNP	missense variant	T/S	126	141	0.14	21	benign	0.02	12001	likely benign	12
19977	SETD2	rs1040670872	SNP	missense variant	A/G	124	331	0.33	6	benign	0.005	5001	likely benign	5
19978	SETD2	rs1445256311	SNP	missense variant	A/T	124	481	0.48	97	benign	0.096	12001	likely benign	12
19979	SETD2	rs1162661952	SNP	missense variant	S/F	121	1	0	936	probably damaging	0.935	22001	likely benign	22
19980	SETD2	rs1404541560	SNP	missense variant	S/P	121	81	0.08	74	benign	0.073	18001	likely benign	18

Left 1997 1998 1999