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
29531	PALB2	rs1555462067	SNP	missense variant	K/Q	47	1	0	894	possibly damaging	0.893	23001	likely benign	23
29532	PALB2	rs756856792	SNP	missense variant	I/M	46	11	0.01	312	benign	0.311	12001	likely benign	12
29533	PALB2	rs551111938	SNP	missense variant	K/N	45	41	0.04	140	benign	0.139	13001	likely benign	13
29534	PALB2	rs765125459	SNP	missense variant	K/E	45	1	0	726	possibly damaging	0.725	24001	likely benign	24
29535	PALB2	rs1064794085	substitution	missense variant	R/I	42	1	0	274	benign	0.273	22001	likely benign	22
29536	PALB2	rs573118236	SNP	missense variant	R/K	42	81	0.08	48	benign	0.047	19001	likely benign	19
29537	PALB2	rs1555462083	SNP	missense variant	Q/L	41	1	0	867	possibly damaging	0.866	23001	likely benign	23
29538	PALB2	rs371875379	SNP	missense variant	A/V	40	1	0	415	benign	0.414	22001	likely benign	22
29539	PALB2	rs371875379	SNP	missense variant	A/G	40	11	0.01	972	probably damaging	0.971	24001	likely benign	24
29540	PALB2	rs202194596	SNP	missense variant	R/L	39	1	0	980	probably damaging	0.979	24001	likely benign	24

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