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
19121	SETD2	rs781155076	SNP	missense variant	N/S	1268	111	0.11	20	benign	0.019	13001	likely benign	13
19122	SETD2	rs559594100	SNP	missense variant	K/E	1267	81	0.08	616	possibly damaging	0.615	22001	likely benign	22
19123	SETD2	rs1469670151	SNP	missense variant	L/V	1265	81	0.08	26	benign	0.025	16001	likely benign	16
19124	SETD2	rs779295786	SNP	missense variant	D/Y	1260	1	0	953	probably damaging	0.952	23001	likely benign	23
19125	SETD2	rs746024449	SNP	missense variant	K/T	1259	1	0	906	possibly damaging	0.905	24001	likely benign	24
19126	SETD2	rs879019101	SNP	missense variant	K/E	1259	171	0.17	750	possibly damaging	0.749	23001	likely benign	23
19127	SETD2	rs912983850	SNP	missense variant	E/K	1257	81	0.08	837	possibly damaging	0.836	22001	likely benign	22
19128	SETD2	rs772220706	SNP	missense variant	A/G	1254	301	0.3	12	benign	0.011	9001	likely benign	9
19129	SETD2	rs779944664	SNP	missense variant	A/S	1254	651	0.65	32	benign	0.031	1	likely benign	0
19130	SETD2	rs747086942	SNP	missense variant	L/S	1253	251	0.25	796	possibly damaging	0.795	14001	likely benign	14

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