Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
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id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
15671	TBX3	rs772620679	SNP	missense variant	A/P	517	41	0.04	906	possibly damaging	0.905	19001	likely benign	19
15672	TBX3	rs772620679	SNP	missense variant	A/T	517	121	0.12	614	possibly damaging	0.613	15001	likely benign	15
15673	TBX3	rs866685357	SNP	missense variant	A/V	515	221	0.22	267	benign	0.266	22001	likely benign	22
15674	TBX3	rs1447833815	SNP	missense variant	M/K	514	1	0	25	benign	0.024	24001	likely benign	24
15675	TBX3	rs200948009	SNP	missense variant	M/V	514	11	0.01	244	benign	0.243	23001	likely benign	23
15676	TBX3	rs566842835	SNP	missense variant	S/N	513	321	0.32	1	benign	0	21001	likely benign	21
15677	TBX3	rs1444457719	SNP	missense variant	A/T	510	41	0.04	211	benign	0.21	24001	likely benign	24
15678	TBX3	rs1370487115	SNP	missense variant	G/A	509	41	0.04	929	probably damaging	0.928	23001	likely benign	23
15679	TBX3	rs1370487115	SNP	missense variant	G/D	509	1	0	978	probably damaging	0.977	24001	likely benign	24
15680	TBX3	rs936879280	SNP	missense variant	M/V	507	41	0.04	26	benign	0.025	23001	likely benign	23

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