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
6771	KM2TC-MLL3	rs201742813	SNP	missense variant	R/H	4608	231	0.23	8	benign	0.007	10001	likely benign	10
6772	KM2TC-MLL3	rs764910946	SNP	missense variant	R/C	4608	61	0.06	826	possibly damaging	0.825	22001	likely benign	22
6773	KM2TC-MLL3	rs1454613804	SNP	missense variant	G/A	4607	61	0.06	999	probably damaging	0.998	22001	likely benign	22
6774	KM2TC-MLL3	rs968112164	SNP	missense variant	D/H	4606	1	0	999	probably damaging	0.998	24001	likely benign	24
6775	KM2TC-MLL3	rs141758280	SNP	missense variant	I/V	4602	361	0.36	937	probably damaging	0.936	23001	likely benign	23
6776	KM2TC-MLL3	rs1483070029	SNP	missense variant	S/A	4601	21	0.02	988	probably damaging	0.987	26001	likely benign	26
6777	KM2TC-MLL3	rs1217182001	SNP	missense variant	R/L	4597	11	0.01	964	probably damaging	0.963	26001	likely benign	26
6778	KM2TC-MLL3	rs1217182001	SNP	missense variant	R/H	4597	71	0.07	501	possibly damaging	0.5	24001	likely benign	24
6779	KM2TC-MLL3	rs543734103	SNP	missense variant	R/C	4597	141	0.14	994	probably damaging	0.993	25001	likely benign	25
6780	KM2TC-MLL3	rs780661300	SNP	missense variant	R/P	4595	1	0	1000	probably damaging	0.999	28001	likely benign	28

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