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
10241	ARID1B	rs1457648775	SNP	missense variant	N/K	108	161	0.16	134	benign	0.133	22001	likely benign	22
10242	ARID1B	rs747743024	SNP	missense variant	Q/R	111	961	0.96	70	benign	0.069	19001	likely benign	19
10243	ARID1B	rs1187066399	SNP	missense variant	Q/H	112	91	0.09	372	benign	0.371	22001	likely benign	22
10244	ARID1B	rs1295182750	SNP	missense variant	Q/P	113	31	0.03	1	benign	0	17001	likely benign	17
10245	ARID1B	rs1341256623	SNP	missense variant	Q/E	114	31	0.03	82	benign	0.081	21001	likely benign	21
10246	ARID1B	rs1438886611	SNP	missense variant	Q/R	121	171	0.17	2	benign	0.001	19001	likely benign	19
10247	ARID1B	rs1291761395	SNP	missense variant	Q/H	121	81	0.08	4	benign	0.003	12001	likely benign	12
10248	ARID1B	rs1209976011	SNP	missense variant	Q/L	123	41	0.04	1	benign	0	22001	likely benign	22
10249	ARID1B	rs970100458	SNP	missense variant	Q/H	123	21	0.02	12	benign	0.011	21001	likely benign	21
10250	ARID1B	rs1003399837	SNP	missense variant	Q/P	124	1	0	1	benign	0	19001	likely benign	19

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