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
30471	AXIN1	rs899023760	SNP	missense variant	T/I	275	101	0.1	202	benign	0.201	23001	likely benign	23
30472	AXIN1	rs899023760	SNP	missense variant	T/R	275	1	0	27	benign	0.026	23001	likely benign	23
30473	AXIN1	rs1431368218	SNP	missense variant	E/Q	274	211	0.21	69	benign	0.068	22001	likely benign	22
30474	AXIN1	rs1012054427	SNP	missense variant	L/V	273	21	0.02	6	benign	0.005	17001	likely benign	17
30475	AXIN1	rs780832517	SNP	missense variant	L/P	271	11	0.01	981	probably damaging	0.98	28001	likely benign	28
30476	AXIN1	rs140151215	SNP	missense variant	Q/E	269	211	0.21	235	benign	0.234	21001	likely benign	21
30477	AXIN1	rs747747465	SNP	missense variant	P/R	268	91	0.09	67	benign	0.066	21001	likely benign	21
30478	AXIN1	rs769359749	SNP	missense variant	P/S	268	331	0.33	2	benign	0.001	6001	likely benign	6
30479	AXIN1	rs200738407	SNP	missense variant	L/R	267	1	0	659	possibly damaging	0.658	25001	likely benign	25
30480	AXIN1	rs374640773	SNP	missense variant	G/A	265	241	0.24	68	benign	0.067	16001	likely benign	16

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