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
17991	BRCA1	rs80357216	SNP	missense variant	V/A	119	91	0.09	889	possibly damaging	0.888	27001	likely benign	27
17992	BRCA1	rs28897698	SNP	missense variant	V/F	119	1	0	951	probably damaging	0.95	25001	likely benign	25
17993	BRCA1	rs28897698	SNP	missense variant	V/I	119	411	0.41	43	benign	0.042	18001	likely benign	18
17994	BRCA1	rs80357358	SNP	missense variant	V/G	118	1	0	994	probably damaging	0.993	31001	likely deleterious	31
17995	BRCA1	rs80357358	SNP	missense variant	V/A	118	1	0	951	probably damaging	0.95	26001	likely benign	26
17996	BRCA1	rs80357358	SNP	missense variant	V/E	118	1	0	985	probably damaging	0.984	27001	likely benign	27
17997	BRCA1	rs1555574756	SNP	missense variant	V/L	118	121	0.12	367	benign	0.366	23001	likely benign	23
17998	BRCA1	rs786202721	SNP	missense variant	I/V	117	1001	1	1	benign	0	1	likely benign	0
17999	BRCA1	rs80357241	SNP	missense variant	P/A	116	821	0.82	1	benign	0	2001	likely benign	2
18000	BRCA1	rs397509281	SNP	missense variant	H/P	115	211	0.21	242	benign	0.241	13001	likely benign	13

Left 1799 1800 1801