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
15571	TBX3	rs189469110	SNP	missense variant	T/I	613	1	0	31	benign	0.03	22001	likely benign	22
15572	TBX3	rs1343061173	SNP	missense variant	T/A	613	331	0.33	1	benign	0	18001	likely benign	18
15573	TBX3	rs1040183921	SNP	missense variant	N/K	612	71	0.07	128	benign	0.127	22001	likely benign	22
15574	TBX3	rs747894358	SNP	missense variant	L/P	611	21	0.02	971	probably damaging	0.97	25001	likely benign	25
15575	TBX3	rs769814877	SNP	missense variant	L/V	611	1	0	721	possibly damaging	0.72	23001	likely benign	23
15576	TBX3	rs769814877	SNP	missense variant	L/M	611	1	0	971	probably damaging	0.97	23001	likely benign	23
15577	TBX3	rs1445898564	SNP	missense variant	N/S	610	431	0.43	4	benign	0.003	18001	likely benign	18
15578	TBX3	rs1259293033	SNP	missense variant	L/F	609	151	0.15	840	possibly damaging	0.839	24001	likely benign	24
15579	TBX3	rs954634731	SNP	missense variant	H/Q	606	81	0.08	602	possibly damaging	0.601	21001	likely benign	21
15580	TBX3	rs1201751425	SNP	missense variant	R/H	605	71	0.07	962	probably damaging	0.961	26001	likely benign	26

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