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
13401	SPEN	rs764181934	SNP	missense variant	V/I	729	51	0.05	79	benign	0.078	20001	likely benign	20
13402	SPEN	rs764181934	SNP	missense variant	V/L	729	41	0.04	58	benign	0.057	21001	likely benign	21
13403	SPEN	rs764181934	SNP	missense variant	V/F	729	11	0.01	361	benign	0.36	22001	likely benign	22
13404	SPEN	rs1230687257	SNP	missense variant	H/D	730	1	0	880	possibly damaging	0.879	25001	likely benign	25
13405	SPEN	rs1374247469	SNP	missense variant	H/Q	730	51	0.05	323	benign	0.322	19001	likely benign	19
13406	SPEN	rs757226572	SNP	missense variant	R/Q	732	1	0	999	probably damaging	0.998	29001	likely benign	29
13407	SPEN	rs138206879	SNP	missense variant	R/C	733	1	0	954	probably damaging	0.953	26001	likely benign	26
13408	SPEN	rs779692614	SNP	missense variant	R/H	733	1	0	117	benign	0.116	24001	likely benign	24
13409	SPEN	rs748929130	SNP	missense variant	P/T	734	81	0.08	13	benign	0.012	16001	likely benign	16
13410	SPEN	rs748929130	SNP	missense variant	P/S	734	11	0.01	256	benign	0.255	21001	likely benign	21

Left 1340 1341 1342