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
10301	ARID1B	rs1207056012	SNP	missense variant	A/V	164	141	0.14	901	possibly damaging	0.9	19001	likely benign	19
10302	ARID1B	rs1022306360	SNP	missense variant	G/D	165	1	0	962	probably damaging	0.961	24001	likely benign	24
10303	ARID1B	rs1022306360	SNP	missense variant	G/A	165	121	0.12	301	benign	0.3	23001	likely benign	23
10304	ARID1B	rs1269347919	SNP	missense variant	G/S	166	1001	1	148	benign	0.147	12001	likely benign	12
10305	ARID1B	rs914813402	SNP	missense variant	D/A	169	11	0.01	141	benign	0.14	22001	likely benign	22
10306	ARID1B	rs1171803835	SNP	missense variant	D/E	169	401	0.4	141	benign	0.14	10001	likely benign	10
10307	ARID1B	rs1171803835	SNP	missense variant	D/E	169	401	0.4	141	benign	0.14	10001	likely benign	10
10308	ARID1B	rs1483839954	SNP	missense variant	P/T	171	11	0.01	974	probably damaging	0.973	21001	likely benign	21
10309	ARID1B	rs1394730320	SNP	missense variant	P/L	171	11	0.01	976	probably damaging	0.975	22001	likely benign	22
10310	ARID1B	rs1430578340	SNP	missense variant	G/D	172	71	0.07	962	probably damaging	0.961	22001	likely benign	22

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