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
26341	MLL2	rs746039927	SNP	missense variant	R/C	348	31	0.03	1	benign	0	24001	likely benign	24
26342	MLL2	rs1020065475	SNP	missense variant	H/R	347	51	0.05	54	benign	0.053	22001	likely benign	22
26343	MLL2	rs770032317	SNP	missense variant	C/S	346	1	0	995	probably damaging	0.994	25001	likely benign	25
26344	MLL2	rs975469976	SNP	missense variant	C/S	346	1	0	995	probably damaging	0.994	25001	likely benign	25
26345	MLL2	rs775685334	SNP	missense variant	L/V	345	1001	1	153	benign	0.152	11001	likely benign	11
26346	MLL2	rs1287920288	SNP	missense variant	S/C	344	51	0.05	721	possibly damaging	0.72	25001	likely benign	25
26347	MLL2	rs1322211105	SNP	missense variant	Y/C	343	291	0.29	951	probably damaging	0.95	23001	likely benign	23
26348	MLL2	rs1488388667	SNP	missense variant	F/L	340	101	0.1	193	benign	0.192	22001	likely benign	22
26349	MLL2	rs1192030302	SNP	missense variant	E/K	338	1	0	38	benign	0.037	23001	likely benign	23
26350	MLL2	rs200245957	SNP	missense variant	S/L	337	41	0.04	4	benign	0.003	23001	likely benign	23

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