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
32171	NOTCH1	rs1325758824	SNP	missense variant	G/S	2345	351	0.35	4	benign	0.003	1	likely benign	0
32172	NOTCH1	rs768695849	SNP	missense variant	Q/L	2343	91	0.09	115	benign	0.114	17001	likely benign	17
32173	NOTCH1	rs1254082910	SNP	missense variant	P/L	2340	211	0.21	22	benign	0.021	15001	likely benign	15
32174	NOTCH1	rs773134608	SNP	missense variant	A/V	2339	201	0.2	119	benign	0.118	14001	likely benign	14
32175	NOTCH1	rs773134608	SNP	missense variant	A/D	2339	281	0.28	210	benign	0.209	14001	likely benign	14
32176	NOTCH1	rs1363351087	SNP	missense variant	S/N	2336	451	0.45	2	benign	0.001	10001	likely benign	10
32177	NOTCH1	rs370135470	SNP	missense variant	P/L	2334	261	0.26	7	benign	0.006	15001	likely benign	15
32178	NOTCH1	rs370135470	SNP	missense variant	P/H	2334	111	0.11	137	benign	0.136	16001	likely benign	16
32179	NOTCH1	rs759916787	SNP	missense variant	P/S	2334	681	0.68	2	benign	0.001	1	likely benign	0
32180	NOTCH1	rs1291495851	SNP	missense variant	P/S	2332	91	0.09	4	benign	0.003	5001	likely benign	5

Left 3217 3218 3219