Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
23021	MLL2	rs1278737777	SNP	missense variant	E/D	4662	291	0.29	4	benign	0.003	15001	likely benign	15
23022	MLL2	rs1031841523	SNP	missense variant	S/R	4661	461	0.46	15	benign	0.014	15001	likely benign	15
23023	MLL2	rs781367864	SNP	missense variant	D/E	4660	821	0.82	4	benign	0.003	2001	likely benign	2
23024	MLL2	rs746244770	SNP	missense variant	D/H	4660	31	0.03	651	possibly damaging	0.65	24001	likely benign	24
23025	MLL2	rs1218766571	SNP	missense variant	R/Q	4659	311	0.31	1	benign	0	17001	likely benign	17
23026	MLL2	rs558561472	SNP	missense variant	R/W	4659	1	0	329	benign	0.328	23001	likely benign	23
23027	MLL2	rs776033634	SNP	missense variant	A/V	4658	71	0.07	632	possibly damaging	0.631	23001	likely benign	23
23028	MLL2	rs1268771491	SNP	missense variant	A/T	4658	171	0.17	92	benign	0.091	19001	likely benign	19
23029	MLL2	rs748791941	SNP	missense variant	S/F	4657	21	0.02	85	benign	0.084	23001	likely benign	23
23030	MLL2	rs748791941	SNP	missense variant	S/C	4657	21	0.02	1	benign	0	22001	likely benign	22

Left 2302 2303 2304