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
19261	SETD2	rs758840930	SNP	missense variant	P/R	1085	101	0.1	544	possibly damaging	0.543	17001	likely benign	17
19262	SETD2	rs1165214835	SNP	missense variant	D/G	1083	181	0.18	73	benign	0.072	19001	likely benign	19
19263	SETD2	rs1419653252	SNP	missense variant	E/G	1082	81	0.08	921	probably damaging	0.92	23001	likely benign	23
19264	SETD2	rs1024800098	SNP	missense variant	F/V	1081	131	0.13	968	probably damaging	0.967	21001	likely benign	21
19265	SETD2	rs766811216	SNP	missense variant	D/G	1080	21	0.02	150	benign	0.149	23001	likely benign	23
19266	SETD2	rs755498169	SNP	missense variant	D/H	1080	11	0.01	986	probably damaging	0.985	23001	likely benign	23
19267	SETD2	rs780702915	SNP	missense variant	Y/C	1077	351	0.35	1001	probably damaging	1	21001	likely benign	21
19268	SETD2	rs780702915	SNP	missense variant	Y/S	1077	211	0.21	1001	probably damaging	1	22001	likely benign	22
19269	SETD2	rs747750475	SNP	missense variant	I/M	1076	131	0.13	26	benign	0.025	14001	likely benign	14
19270	SETD2	rs554338477	SNP	missense variant	I/V	1076	651	0.65	2	benign	0.001	1	likely benign	0

Left 1926 1927 1928