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
10361	ARID1B	rs1294837845	SNP	missense variant	G/S	239	161	0.16	148	benign	0.147	17001	likely benign	17
10362	ARID1B	rs1294837845	SNP	missense variant	G/C	239	1	0	988	probably damaging	0.987	23001	likely benign	23
10363	ARID1B	rs1445103954	SNP	missense variant	G/A	239	21	0.02	94	benign	0.093	22001	likely benign	22
10364	ARID1B	rs1332589796	SNP	missense variant	G/C	240	1	0	998	probably damaging	0.997	24001	likely benign	24
10365	ARID1B	rs1480645552	SNP	missense variant	P/S	241	51	0.05	240	benign	0.239	21001	likely benign	21
10366	ARID1B	rs775385239	SNP	missense variant	P/R	241	11	0.01	216	benign	0.215	22001	likely benign	22
10367	ARID1B	rs1277576104	SNP	missense variant	G/V	242	1	0	974	probably damaging	0.973	22001	likely benign	22
10368	ARID1B	rs375160616	SNP	missense variant	G/S	243	121	0.12	504	possibly damaging	0.503	22001	likely benign	22
10369	ARID1B	rs768554794	SNP	missense variant	R/P	244	1	0	233	benign	0.232	23001	likely benign	23
10370	ARID1B	rs1562376815	SNP	missense variant	G/A	246	1	0	970	probably damaging	0.969	22001	likely benign	22

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