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
6321	CDH1	rs587782838	SNP	missense variant	I/V	614	221	0.22	386	benign	0.385	20001	likely benign	20
6322	CDH1	rs587782838	SNP	missense variant	I/F	614	1	0	902	possibly damaging	0.901	25001	likely benign	25
6323	CDH1	rs1003012321	SNP	missense variant	I/V	615	541	0.54	7	benign	0.006	3001	likely benign	3
6324	CDH1	rs760707493	SNP	missense variant	I/T	615	1001	1	20	benign	0.019	5001	likely benign	5
6325	CDH1	rs33935154	SNP	missense variant	A/T	617	81	0.08	54	benign	0.053	15001	likely benign	15
6326	CDH1	rs33935154	SNP	missense variant	A/S	617	121	0.12	7	benign	0.006	13001	likely benign	13
6327	CDH1	rs876659221	SNP	missense variant	L/F	619	101	0.1	924	probably damaging	0.923	23001	likely benign	23
6328	CDH1	rs786201888	SNP	missense variant	P/T	620	91	0.09	720	possibly damaging	0.719	22001	likely benign	22
6329	CDH1	rs786201888	SNP	missense variant	P/S	620	281	0.28	55	benign	0.054	18001	likely benign	18
6330	CDH1	rs1555516871	SNP	missense variant	P/L	620	11	0.01	867	possibly damaging	0.866	25001	likely benign	25

Left 632 633 634