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
12221	CCNE1	rs745919586	SNP	missense variant	R/L	27	21	0.02	998	probably damaging	0.997	29001	likely benign	29
12222	CCNE1	rs145289511	SNP	missense variant	S/F	28	1	0	642	possibly damaging	0.641	28001	likely benign	28
12223	CCNE1	rs1205916639	SNP	missense variant	K/R	30	11	0.01	995	probably damaging	0.994	32001	likely deleterious	32
12224	CCNE1	rs1443126704	SNP	missense variant	R/G	31	1	0	995	probably damaging	0.994	34001	likely deleterious	34
12225	CCNE1	rs1437724105	SNP	missense variant	A/T	33	41	0.04	708	possibly damaging	0.707	32001	likely deleterious	32
12226	CCNE1	rs1186891855	SNP	missense variant	A/V	33	51	0.05	708	possibly damaging	0.707	34001	likely deleterious	34
12227	CCNE1	rs763083338	SNP	missense variant	N/K	34	41	0.04	137	benign	0.136	24001	likely benign	24
12228	CCNE1	rs369751087	SNP	missense variant	V/M	35	1	0	999	probably damaging	0.998	32001	likely deleterious	32
12229	CCNE1	rs1355673586	SNP	missense variant	T/A	36	1001	1	1	benign	0	21001	likely benign	21
12230	CCNE1	rs1472595244	SNP	missense variant	T/N	36	11	0.01	86	benign	0.085	23001	likely benign	23

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