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
30041	AXIN1	rs1034818030	SNP	missense variant	Y/H	752	1	0	995	probably damaging	0.994	26001	likely benign	26
30042	AXIN1	rs761321644	SNP	missense variant	A/V	750	101	0.1	285	benign	0.284	25001	likely benign	25
30043	AXIN1	rs370509578	SNP	missense variant	V/M	749	1	0	1001	probably damaging	1	24001	likely benign	24
30044	AXIN1	rs1220971406	SNP	missense variant	V/A	748	61	0.06	374	benign	0.373	24001	likely benign	24
30045	AXIN1	rs777185421	SNP	missense variant	V/F	748	1	0	940	probably damaging	0.939	24001	likely benign	24
30046	AXIN1	rs777185421	SNP	missense variant	V/L	748	11	0.01	213	benign	0.212	23001	likely benign	23
30047	AXIN1	rs777185421	SNP	missense variant	V/I	748	61	0.06	180	benign	0.179	22001	likely benign	22
30048	AXIN1	rs370965851	SNP	missense variant	I/M	747	131	0.13	430	benign	0.429	7001	likely benign	7
30049	AXIN1	rs752402029	SNP	missense variant	I/T	747	221	0.22	245	benign	0.244	23001	likely benign	23
30050	AXIN1	rs1567256688	SNP	missense variant	S/R	746	61	0.06	190	benign	0.189	24001	likely benign	24

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