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
941	MYC	rs1194568592	SNP	missense variant	P/L	206	21	0.02	991	probably damaging	0.99	32001	likely deleterious	32
942	MYC	rs1221801220	SNP	missense variant	P/R	213	1	0	1001	probably damaging	1	26001	likely benign	26
943	MYC	rs1429861982	SNP	missense variant	L/F	214	41	0.04	983	probably damaging	0.982	25001	likely benign	25
944	MYC	rs753502487	SNP	missense variant	N/K	215	561	0.56	69	benign	0.068	14001	likely benign	14
945	MYC	rs577698378	SNP	missense variant	D/N	216	71	0.07	653	possibly damaging	0.652	23001	likely benign	23
946	MYC	rs778262855	SNP	missense variant	D/G	216	121	0.12	536	possibly damaging	0.535	22001	likely benign	22
947	MYC	rs922203242	SNP	missense variant	S/N	217	341	0.34	833	possibly damaging	0.832	18001	likely benign	18
948	MYC	rs754835412	SNP	missense variant	S/P	219	291	0.29	215	benign	0.214	22001	likely benign	22
949	MYC	rs112602073	SNP	missense variant	P/S	220	41	0.04	136	benign	0.135	24001	likely benign	24
950	MYC	rs1041258616	SNP	missense variant	P/R	220	41	0.04	902	possibly damaging	0.901	25001	likely benign	25

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