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
30401	AXIN1	rs970119890	SNP	missense variant	V/M	366	1	0	679	possibly damaging	0.678	24001	likely benign	24
30402	AXIN1	rs200837956	SNP	missense variant	R/Q	365	1001	1	297	benign	0.296	18001	likely benign	18
30403	AXIN1	rs1324067997	SNP	missense variant	R/W	365	1	0	987	probably damaging	0.986	25001	likely benign	25
30404	AXIN1	rs1207683443	SNP	missense variant	G/R	364	1	0	773	possibly damaging	0.772	25001	likely benign	25
30405	AXIN1	rs1207683443	SNP	missense variant	G/R	364	1	0	773	possibly damaging	0.772	25001	likely benign	25
30406	AXIN1	rs771361430	SNP	missense variant	N/S	363	1	0	227	benign	0.226	26001	likely benign	26
30407	AXIN1	rs777137467	SNP	missense variant	V/I	362	141	0.14	64	benign	0.063	21001	likely benign	21
30408	AXIN1	rs759808424	SNP	missense variant	V/L	360	21	0.02	4	benign	0.003	17001	likely benign	17
30409	AXIN1	rs759808424	SNP	missense variant	V/M	360	161	0.16	214	benign	0.213	15001	likely benign	15
30410	AXIN1	rs1439391940	SNP	missense variant	S/N	359	121	0.12	814	possibly damaging	0.813	22001	likely benign	22

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