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
15981	TBX3	rs927204453	SNP	missense variant	V/F	124	1	0	1000	probably damaging	0.999	29001	likely benign	29
15982	TBX3	rs927204453	SNP	missense variant	V/I	124	131	0.13	784	possibly damaging	0.783	27001	likely benign	27
15983	TBX3	rs1373707233	SNP	missense variant	G/A	120	1	0	996	probably damaging	0.995	26001	likely benign	26
15984	TBX3	rs985381779	SNP	missense variant	G/C	120	1	0	1001	probably damaging	1	29001	likely benign	29
15985	TBX3	rs746495505	SNP	missense variant	D/V	114	1	0	350	benign	0.349	29001	likely benign	29
15986	TBX3	rs772441761	SNP	missense variant	D/H	114	1	0	828	possibly damaging	0.827	27001	likely benign	27
15987	TBX3	rs772441761	SNP	missense variant	D/N	114	71	0.07	92	benign	0.091	23001	likely benign	23
15988	TBX3	rs1314068240	SNP	missense variant	H/Q	106	311	0.31	661	possibly damaging	0.66	23001	likely benign	23
15989	TBX3	rs776626691	SNP	missense variant	H/Y	106	1001	1	115	benign	0.114	23001	likely benign	23
15990	TBX3	rs150806908	SNP	missense variant	K/R	104	21	0.02	980	probably damaging	0.979	29001	likely benign	29

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