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
9821	KM2TC-MLL3	rs750849305	SNP	missense variant	D/G	457	71	0.07	816	possibly damaging	0.815	24001	likely benign	24
9822	KM2TC-MLL3	rs1463520557	SNP	missense variant	C/R	456	1	0	998	probably damaging	0.997	27001	likely benign	27
9823	KM2TC-MLL3	rs77652527	SNP	missense variant	I/M	455	251	0.25	4	benign	0.003	14001	likely benign	14
9824	KM2TC-MLL3	rs534592021	SNP	missense variant	I/V	455	1001	1	1	benign	0	13001	likely benign	13
9825	KM2TC-MLL3	rs534592021	SNP	missense variant	I/L	455	931	0.93	1	benign	0	14001	likely benign	14
9826	KM2TC-MLL3	rs1454772066	SNP	missense variant	N/K	452	1	0	256	benign	0.255	22001	likely benign	22
9827	KM2TC-MLL3	rs201023756	SNP	missense variant	N/S	452	21	0.02	22	benign	0.021	22001	likely benign	22
9828	KM2TC-MLL3	rs934365973	SNP	missense variant	H/R	451	1	0	853	possibly damaging	0.852	24001	likely benign	24
9829	KM2TC-MLL3	rs1376200985	SNP	missense variant	H/Y	450	101	0.1	995	probably damaging	0.994	24001	likely benign	24
9830	KM2TC-MLL3	rs149250254	SNP	missense variant	Q/H	448	1	0	43	benign	0.042	22001	likely benign	22

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