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
16011	TBX3	rs1372676946	SNP	missense variant	S/A	80	701	0.7	44	benign	0.043	22001	likely benign	22
16012	TBX3	rs770004469	SNP	missense variant	P/R	77	181	0.18	524	possibly damaging	0.523	25001	likely benign	25
16013	TBX3	rs1310081694	SNP	missense variant	I/N	76	21	0.02	808	possibly damaging	0.807	29001	likely benign	29
16014	TBX3	rs866573295	SNP	missense variant	G/D	75	11	0.01	965	probably damaging	0.964	26001	likely benign	26
16015	TBX3	rs895278286	SNP	missense variant	G/R	75	21	0.02	986	probably damaging	0.985	28001	likely benign	28
16016	TBX3	rs895278286	SNP	missense variant	G/S	75	11	0.01	620	possibly damaging	0.619	27001	likely benign	27
16017	TBX3	rs1266535166	SNP	missense variant	E/K	73	11	0.01	975	probably damaging	0.974	24001	likely benign	24
16018	TBX3	rs1012420316	SNP	missense variant	A/S	71	41	0.04	973	probably damaging	0.972	26001	likely benign	26
16019	TBX3	rs1012420316	SNP	missense variant	A/T	71	11	0.01	993	probably damaging	0.992	27001	likely benign	27
16020	TBX3	rs1006993913	SNP	missense variant	G/W	70	1	0	1001	probably damaging	1	32001	likely deleterious	32

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