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
19211	SETD2	rs776438900	SNP	missense variant	T/A	1142	1	0	1000	probably damaging	0.999	25001	likely benign	25
19212	SETD2	rs769596273	SNP	missense variant	T/I	1141	1	0	946	probably damaging	0.945	23001	likely benign	23
19213	SETD2	rs769596273	SNP	missense variant	T/S	1141	1001	1	118	benign	0.117	15001	likely benign	15
19214	SETD2	rs773098323	SNP	missense variant	S/F	1140	1	0	374	benign	0.373	23001	likely benign	23
19215	SETD2	rs773098323	SNP	missense variant	S/C	1140	1	0	474	possibly damaging	0.473	23001	likely benign	23
19216	SETD2	rs762731738	SNP	missense variant	P/L	1139	1	0	1001	probably damaging	1	27001	likely benign	27
19217	SETD2	rs1385858883	SNP	missense variant	K/R	1138	71	0.07	20	benign	0.019	21001	likely benign	21
19218	SETD2	rs767782860	SNP	missense variant	K/E	1138	1	0	394	benign	0.393	23001	likely benign	23
19219	SETD2	rs371514512	SNP	missense variant	E/G	1137	1	0	1000	probably damaging	0.999	24001	likely benign	24
19220	SETD2	rs1337050438	SNP	missense variant	E/K	1137	11	0.01	1000	probably damaging	0.999	23001	likely benign	23

Left 1921 1922 1923