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
27891	PDGFFRA	rs764472307	SNP	missense variant	A/E	7	251	0.25	39	benign	0.038	3001	likely benign	3
27892	PDGFFRA	rs764472307	SNP	missense variant	A/V	7	551	0.55	1	benign	0	5001	likely benign	5
27893	PDGFFRA	rs1060501519	SNP	missense variant	V/I	10	991	0.99	2	benign	0.001	8001	likely benign	8
27894	PDGFFRA	rs781404006	SNP	missense variant	V/D	10	1	0	468	possibly damaging	0.467	23001	likely benign	23
27895	PDGFFRA	rs1440200916	SNP	missense variant	G/A	12	521	0.52	24	benign	0.023	16001	likely benign	16
27896	PDGFFRA	rs1440200916	SNP	missense variant	G/V	12	301	0.3	4	benign	0.003	21001	likely benign	21
27897	PDGFFRA	rs1227672940	SNP	missense variant	C/Y	13	391	0.39	1	benign	0	18001	likely benign	18
27898	PDGFFRA	rs1286350038	SNP	missense variant	L/P	15	41	0.04	581	possibly damaging	0.58	25001	likely benign	25
27899	PDGFFRA	rs587778596	SNP	missense variant	T/S	16	341	0.34	2	benign	0.001	11001	likely benign	11
27900	PDGFFRA	rs766600687	SNP	missense variant	G/V	17	11	0.01	599	possibly damaging	0.598	13001	likely benign	13

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