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
18341	CTCF	rs1386847711	SNP	missense variant	D/H	222	11	0.01	996	probably damaging	0.995	27001	likely benign	27
18342	CTCF	rs772804334	SNP	missense variant	D/N	227	291	0.29	986	probably damaging	0.985	24001	likely benign	24
18343	CTCF	rs370955794	SNP	missense variant	Q/L	232	11	0.01	933	probably damaging	0.932	26001	likely benign	26
18344	CTCF	rs373979002	SNP	missense variant	E/D	234	71	0.07	957	probably damaging	0.956	22001	likely benign	22
18345	CTCF	rs1478115407	SNP	missense variant	V/I	240	81	0.08	957	probably damaging	0.956	24001	likely benign	24
18346	CTCF	rs758579289	SNP	missense variant	V/M	245	21	0.02	855	possibly damaging	0.854	26001	likely benign	26
18347	CTCF	rs777993880	SNP	missense variant	V/A	246	131	0.13	485	possibly damaging	0.484	23001	likely benign	23
18348	CTCF	rs1318657076	SNP	missense variant	G/V	247	21	0.02	809	possibly damaging	0.808	25001	likely benign	25
18349	CTCF	rs747052464	SNP	missense variant	M/V	249	121	0.12	268	benign	0.267	21001	likely benign	21
18350	CTCF	rs1213153569	SNP	missense variant	K/R	256	251	0.25	22	benign	0.021	22001	likely benign	22

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