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
27981	PDGFFRA	rs574683248	SNP	missense variant	V/M	140	21	0.02	214	benign	0.213	22001	likely benign	22
27982	PDGFFRA	rs574683248	SNP	missense variant	V/L	140	481	0.48	1	benign	0	17001	likely benign	17
27983	PDGFFRA	rs757790893	SNP	missense variant	E/A	141	471	0.47	25	benign	0.024	20001	likely benign	20
27984	PDGFFRA	rs1187957560	SNP	missense variant	E/D	141	341	0.34	1	benign	0	8001	likely benign	8
27985	PDGFFRA	rs1337241636	SNP	missense variant	D/G	142	221	0.22	1	benign	0	20001	likely benign	20
27986	PDGFFRA	rs1337241636	SNP	missense variant	D/V	142	61	0.06	23	benign	0.022	19001	likely benign	19
27987	PDGFFRA	rs201614191	SNP	missense variant	D/E	142	1001	1	1	benign	0	1	likely benign	0
27988	PDGFFRA	rs1553902692	SNP	missense variant	D/E	143	461	0.46	1	benign	0	7001	likely benign	7
27989	PDGFFRA	rs376497743	SNP	missense variant	D/Y	144	11	0.01	657	possibly damaging	0.656	28001	likely benign	28
27990	PDGFFRA	rs770117588	SNP	missense variant	D/G	144	161	0.16	85	benign	0.084	22001	likely benign	22

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