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
31681	MLH1	rs1360598779	SNP	missense variant	P/T	438	61	0.06	906	possibly damaging	0.905	22001	likely benign	22
31682	MLH1	rs1553658032	SNP	missense variant	P/L	438	31	0.03	395	benign	0.394	23001	likely benign	23
31683	MLH1	rs1559575214	SNP	missense variant	W/G	440	81	0.08	156	benign	0.155	24001	likely benign	24
31684	MLH1	rs1559575256	SNP	missense variant	A/S	441	81	0.08	178	benign	0.177	22001	likely benign	22
31685	MLH1	rs267607843	SNP	missense variant	A/D	441	1	0	835	possibly damaging	0.834	25001	likely benign	25
31686	MLH1	rs1064793578	SNP	missense variant	A/P	443	11	0.01	492	possibly damaging	0.491	26001	likely benign	26
31687	MLH1	rs757728402	SNP	missense variant	A/V	443	551	0.55	1	benign	0	20001	likely benign	20
31688	MLH1	rs63750511	SNP	missense variant	Q/P	444	1	0	1001	probably damaging	1	28001	likely benign	28
31689	MLH1	rs63750511	SNP	missense variant	Q/L	444	1	0	999	probably damaging	0.998	28001	likely benign	28
31690	MLH1	rs1295425666	SNP	missense variant	H/Y	445	451	0.45	13	benign	0.012	20001	likely benign	20

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