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
24181	MLL2	rs773164595	SNP	missense variant	R/C	3110	1	0	549	possibly damaging	0.548	24001	likely benign	24
24182	MLL2	rs762516845	SNP	missense variant	P/H	3109	21	0.02	86	benign	0.085	22001	likely benign	22
24183	MLL2	rs1435661942	SNP	missense variant	P/S	3109	151	0.15	1	benign	0	12001	likely benign	12
24184	MLL2	rs761708546	SNP	missense variant	A/T	3106	121	0.12	1	benign	0	11001	likely benign	11
24185	MLL2	rs187278562	SNP	missense variant	D/V	3105	11	0.01	7	benign	0.006	21001	likely benign	21
24186	MLL2	rs755031010	SNP	missense variant	A/V	3103	121	0.12	1	benign	0	13001	likely benign	13
24187	MLL2	rs970061739	SNP	missense variant	P/L	3102	41	0.04	26	benign	0.025	22001	likely benign	22
24188	MLL2	rs892233811	SNP	missense variant	P/A	3102	71	0.07	1	benign	0	14001	likely benign	14
24189	MLL2	rs1271758887	SNP	missense variant	P/L	3101	341	0.34	37	benign	0.036	15001	likely benign	15
24190	MLL2	rs1179293337	SNP	missense variant	P/S	3100	141	0.14	47	benign	0.046	17001	likely benign	17

Left 2418 2419 2420