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
2331	ZNF703	rs1341299586	SNP	missense variant	P/T	76	1	0	984	probably damaging	0.983	26001	likely benign	26
2332	ZNF703	rs368977849	SNP	missense variant	P/L	76	1	0	946	probably damaging	0.945	29001	likely benign	29
2333	ZNF703	rs1181846365	SNP	missense variant	P/L	79	31	0.03	942	probably damaging	0.941	26001	likely benign	26
2334	ZNF703	rs1245091054	SNP	missense variant	I/T	80	71	0.07	936	probably damaging	0.935	25001	likely benign	25
2335	ZNF703	rs76445150	SNP	missense variant	D/E	83	1	0	977	probably damaging	0.976	25001	likely benign	25
2336	ZNF703	rs1258989840	SNP	missense variant	A/T	84	21	0.02	993	probably damaging	0.992	29001	likely benign	29
2337	ZNF703	rs756603560	SNP	missense variant	K/E	85	21	0.02	519	possibly damaging	0.518	27001	likely benign	27
2338	ZNF703	rs1489979802	SNP	missense variant	P/S	88	1	0	1000	probably damaging	0.999	26001	likely benign	26
2339	ZNF703	rs941059164	SNP	missense variant	A/E	90	1	0	989	probably damaging	0.988	26001	likely benign	26
2340	ZNF703	rs941059164	SNP	missense variant	A/V	90	21	0.02	708	possibly damaging	0.707	25001	likely benign	25

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