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
3521	RB1	rs1060503083	SNP	missense variant	V/F	742	1	0	1001	probably damaging	1	29001	likely benign	29
3522	RB1	rs1306675913	SNP	missense variant	I/V	744	11	0.01	305	benign	0.304	23001	likely benign	23
3523	RB1	rs958914211	SNP	missense variant	E/Q	746	21	0.02	879	possibly damaging	0.878	28001	likely benign	28
3524	RB1	rs3092905	SNP	missense variant	E/G	746	111	0.11	198	benign	0.197	23001	likely benign	23
3525	RB1	rs767200255	SNP	missense variant	E/A	747	341	0.34	113	benign	0.112	22001	likely benign	22
3526	RB1	rs750057315	SNP	missense variant	E/D	747	441	0.44	62	benign	0.061	14001	likely benign	14
3527	RB1	rs121913297	SNP	missense variant	E/K	748	201	0.2	18	benign	0.017	22001	likely benign	22
3528	RB1	rs1555294601	SNP	missense variant	I/L	752	121	0.12	967	probably damaging	0.966	24001	likely benign	24
3529	RB1	rs1555294601	SNP	missense variant	I/V	752	41	0.04	953	probably damaging	0.952	25001	likely benign	25
3530	RB1	rs587778642	SNP	missense variant	V/I	754	31	0.03	180	benign	0.179	23001	likely benign	23

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