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
15961	TBX3	rs754023417	SNP	missense variant	E/K	179	1	0	988	probably damaging	0.987	28001	likely benign	28
15962	TBX3	rs1299722140	SNP	missense variant	A/T	173	21	0.02	989	probably damaging	0.988	28001	likely benign	28
15963	TBX3	rs745631586	SNP	missense variant	V/M	172	1	0	1000	probably damaging	0.999	27001	likely benign	27
15964	TBX3	rs905399897	SNP	missense variant	M/L	171	61	0.06	425	benign	0.424	27001	likely benign	27
15965	TBX3	rs772182165	SNP	missense variant	R/L	169	1	0	995	probably damaging	0.994	29001	likely benign	29
15966	TBX3	rs772182165	SNP	missense variant	R/Q	169	41	0.04	995	probably damaging	0.994	31001	likely deleterious	31
15967	TBX3	rs1430142395	SNP	missense variant	R/W	169	1	0	1001	probably damaging	1	33001	likely deleterious	33
15968	TBX3	rs1565861840	SNP	missense variant	R/H	162	1	0	996	probably damaging	0.995	31001	likely deleterious	31
15969	TBX3	rs1285766986	SNP	missense variant	I/T	156	31	0.03	38	benign	0.037	24001	likely benign	24
15970	TBX3	rs761429570	SNP	missense variant	I/V	156	1001	1	1	benign	0	18001	likely benign	18

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