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
19171	SETD2	rs1476602371	SNP	missense variant	Q/R	1196	91	0.09	999	probably damaging	0.998	23001	likely benign	23
19172	SETD2	rs147170912	SNP	missense variant	R/Q	1194	31	0.03	262	benign	0.261	24001	likely benign	24
19173	SETD2	rs200956000	SNP	missense variant	V/L	1191	651	0.65	50	benign	0.049	3001	likely benign	3
19174	SETD2	rs200956000	SNP	missense variant	V/M	1191	241	0.24	88	benign	0.087	7001	likely benign	7
19175	SETD2	rs950016449	SNP	missense variant	G/A	1189	571	0.57	105	benign	0.104	12001	likely benign	12
19176	SETD2	rs950016449	SNP	missense variant	G/E	1189	181	0.18	160	benign	0.159	15001	likely benign	15
19177	SETD2	rs1239696144	SNP	missense variant	G/V	1187	51	0.05	1001	probably damaging	1	24001	likely benign	24
19178	SETD2	rs1429220590	SNP	missense variant	P/L	1186	41	0.04	787	possibly damaging	0.786	22001	likely benign	22
19179	SETD2	rs377488968	SNP	missense variant	P/S	1186	31	0.03	171	benign	0.17	20001	likely benign	20
19180	SETD2	rs377488968	SNP	missense variant	P/A	1186	161	0.16	74	benign	0.073	15001	likely benign	15

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