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
1551	ERBB2	rs370959592	SNP	missense variant	P/L	122	351	0.35	1	benign	0	6001	likely benign	6
1552	ERBB2	rs1283546661	SNP	missense variant	N/Y	124	141	0.14	291	benign	0.29	17001	likely benign	17
1553	ERBB2	rs970583285	SNP	missense variant	T/P	127	131	0.13	13	benign	0.012	11001	likely benign	11
1554	ERBB2	rs761564667	SNP	missense variant	P/A	128	371	0.37	1	benign	0	1001	likely benign	1
1555	ERBB2	rs373824622	SNP	missense variant	P/R	128	231	0.23	125	benign	0.124	12001	likely benign	12
1556	ERBB2	rs766949725	SNP	missense variant	V/F	129	681	0.68	79	benign	0.078	11001	likely benign	11
1557	ERBB2	rs754295165	SNP	missense variant	P/S	134	781	0.78	4	benign	0.003	8001	likely benign	8
1558	ERBB2	rs865925114	SNP	missense variant	P/Q	134	601	0.6	4	benign	0.003	11001	likely benign	11
1559	ERBB2	rs755427616	SNP	missense variant	G/S	136	1	0	996	probably damaging	0.995	27001	likely benign	27
1560	ERBB2	rs200208742	SNP	missense variant	L/Q	137	1	0	998	probably damaging	0.997	27001	likely benign	27

Left 155 156 157