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
17601	CDK6	rs753943224	SNP	missense variant	V/I	112	41	0.04	130	benign	0.129	23001	likely benign	23
17602	CDK6	rs757348412	SNP	missense variant	K/E	111	21	0.02	822	possibly damaging	0.821	28001	likely benign	28
17603	CDK6	rs1200123700	SNP	missense variant	D/G	110	31	0.03	113	benign	0.112	25001	likely benign	25
17604	CDK6	rs35654944	SNP	missense variant	D/N	110	111	0.11	4	benign	0.003	22001	likely benign	22
17605	CDK6	rs1178575524	SNP	missense variant	D/N	102	31	0.03	878	possibly damaging	0.877	27001	likely benign	27
17606	CDK6	rs747411819	SNP	missense variant	K/R	93	301	0.3	10	benign	0.009	22001	likely benign	22
17607	CDK6	rs769128722	SNP	missense variant	T/A	92	561	0.56	762	possibly damaging	0.761	23001	likely benign	23
17608	CDK6	rs1397500696	SNP	missense variant	E/D	91	81	0.08	66	benign	0.065	18001	likely benign	18
17609	CDK6	rs777062207	SNP	missense variant	R/G	90	101	0.1	922	probably damaging	0.921	23001	likely benign	23
17610	CDK6	rs1284606692	SNP	missense variant	D/V	89	11	0.01	499	possibly damaging	0.498	27001	likely benign	27

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