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
11821	ARID1A	rs749910396	SNP	missense variant	A/P	79	191	0.19	792	possibly damaging	0.791	22001	likely benign	22
11822	ARID1A	rs757871618	SNP	missense variant	A/V	79	331	0.33	32	benign	0.031	20001	likely benign	20
11823	ARID1A	rs151074395	SNP	missense variant	P/A	80	61	0.06	512	possibly damaging	0.511	22001	likely benign	22
11824	ARID1A	rs151074395	SNP	missense variant	P/S	80	71	0.07	122	benign	0.121	23001	likely benign	23
11825	ARID1A	rs1358984536	SNP	missense variant	P/L	80	51	0.05	840	possibly damaging	0.839	25001	likely benign	25
11826	ARID1A	rs893433709	SNP	missense variant	A/P	81	931	0.93	12	benign	0.011	10001	likely benign	10
11827	ARID1A	rs755377273	SNP	missense variant	P/S	82	211	0.21	359	benign	0.358	20001	likely benign	20
11828	ARID1A	rs372335126	SNP	missense variant	P/A	85	161	0.16	779	possibly damaging	0.778	20001	likely benign	20
11829	ARID1A	rs372335126	SNP	missense variant	P/S	85	191	0.19	843	possibly damaging	0.842	19001	likely benign	19
11830	ARID1A	rs1217038062	SNP	missense variant	P/L	85	71	0.07	945	probably damaging	0.944	22001	likely benign	22

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