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
19101	SETD2	rs370129587	SNP	missense variant	R/S	1296	171	0.17	1000	probably damaging	0.999	21001	likely benign	21
19102	SETD2	rs587778677	SNP	missense variant	L/P	1293	241	0.24	160	benign	0.159	22001	likely benign	22
19103	SETD2	rs762132169	SNP	missense variant	S/I	1289	1	0	1000	probably damaging	0.999	24001	likely benign	24
19104	SETD2	rs762132169	SNP	missense variant	S/N	1289	181	0.18	1000	probably damaging	0.999	19001	likely benign	19
19105	SETD2	rs1014469298	SNP	missense variant	E/G	1288	1	0	1000	probably damaging	0.999	27001	likely benign	27
19106	SETD2	rs373340813	SNP	missense variant	D/H	1286	1	0	988	probably damaging	0.987	25001	likely benign	25
19107	SETD2	rs750062275	SNP	missense variant	S/G	1285	1	0	999	probably damaging	0.998	25001	likely benign	25
19108	SETD2	rs1256168074	SNP	missense variant	R/G	1279	1	0	1000	probably damaging	0.999	24001	likely benign	24
19109	SETD2	rs1346378722	SNP	missense variant	K/N	1278	1	0	1001	probably damaging	1	24001	likely benign	24
19110	SETD2	rs765767219	SNP	missense variant	L/F	1276	31	0.03	838	possibly damaging	0.837	23001	likely benign	23

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