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
2371	ZNF703	rs1024549984	SNP	missense variant	R/H	128	61	0.06	63	benign	0.062	22001	likely benign	22
2372	ZNF703	rs866552378	SNP	missense variant	A/P	130	311	0.31	407	benign	0.406	13001	likely benign	13
2373	ZNF703	rs889595220	SNP	missense variant	A/D	130	701	0.7	19	benign	0.018	8001	likely benign	8
2374	ZNF703	rs1253600019	SNP	missense variant	P/L	131	1	0	10	benign	0.009	20001	likely benign	20
2375	ZNF703	rs764595172	SNP	missense variant	G/S	132	531	0.53	126	benign	0.125	17001	likely benign	17
2376	ZNF703	rs754246446	SNP	missense variant	G/D	132	411	0.41	44	benign	0.043	18001	likely benign	18
2377	ZNF703	rs778822956	SNP	missense variant	A/T	133	391	0.39	98	benign	0.097	17001	likely benign	17
2378	ZNF703	rs1426519307	SNP	missense variant	A/T	134	611	0.61	520	possibly damaging	0.519	18001	likely benign	18
2379	ZNF703	rs1426519307	SNP	missense variant	A/S	134	781	0.78	92	benign	0.091	12001	likely benign	12
2380	ZNF703	rs758679664	SNP	missense variant	A/S	136	1001	1	92	benign	0.091	15001	likely benign	15

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