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
22941	MLL2	rs1287655568	SNP	missense variant	V/A	4801	1001	1	20	benign	0.019	20001	likely benign	20
22942	MLL2	rs373731411	SNP	missense variant	V/M	4799	31	0.03	57	benign	0.056	23001	likely benign	23
22943	MLL2	rs775548388	SNP	missense variant	A/T	4792	1	0	997	probably damaging	0.996	27001	likely benign	27
22944	MLL2	rs1237654242	SNP	missense variant	A/T	4791	321	0.32	863	possibly damaging	0.862	24001	likely benign	24
22945	MLL2	rs895080026	SNP	missense variant	A/S	4790	441	0.44	160	benign	0.159	21001	likely benign	21
22946	MLL2	rs1011898577	SNP	missense variant	M/I	4785	171	0.17	345	benign	0.344	22001	likely benign	22
22947	MLL2	rs763182228	SNP	missense variant	M/T	4785	651	0.65	13	benign	0.012	20001	likely benign	20
22948	MLL2	rs764253212	SNP	missense variant	S/N	4780	521	0.52	24	benign	0.023	20001	likely benign	20
22949	MLL2	rs1220652471	SNP	missense variant	S/R	4780	91	0.09	8	benign	0.007	23001	likely benign	23
22950	MLL2	rs1263198421	SNP	missense variant	G/A	4779	121	0.12	183	benign	0.182	22001	likely benign	22

Left 2294 2295 2296