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
15971	TBX3	rs1296731331	SNP	missense variant	I/V	155	51	0.05	952	probably damaging	0.951	26001	likely benign	26
15972	TBX3	rs1312105333	SNP	missense variant	A/V	147	11	0.01	993	probably damaging	0.992	31001	likely deleterious	31
15973	TBX3	rs1312105333	SNP	missense variant	A/D	147	1	0	998	probably damaging	0.997	31001	likely deleterious	31
15974	TBX3	rs1256655578	SNP	missense variant	K/R	145	81	0.08	544	possibly damaging	0.543	25001	likely benign	25
15975	TBX3	rs769431199	SNP	missense variant	D/E	144	61	0.06	898	possibly damaging	0.897	26001	likely benign	26
15976	TBX3	rs1206189010	SNP	missense variant	L/M	143	31	0.03	967	probably damaging	0.966	26001	likely benign	26
15977	TBX3	rs774747599	SNP	missense variant	F/L	136	41	0.04	922	probably damaging	0.921	32001	likely deleterious	32
15978	TBX3	rs267603321	SNP	missense variant	P/S	135	121	0.12	937	probably damaging	0.936	25001	likely benign	25
15979	TBX3	rs370785408	SNP	missense variant	M/V	132	1	0	980	probably damaging	0.979	26001	likely benign	26
15980	TBX3	rs1201988110	SNP	missense variant	R/G	131	11	0.01	999	probably damaging	0.998	26001	likely benign	26

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