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
24221	MLL2	rs764280781	SNP	missense variant	A/V	3010	141	0.14	992	probably damaging	0.991	23001	likely benign	23
24222	MLL2	rs764280781	SNP	missense variant	A/G	3010	51	0.05	988	probably damaging	0.987	24001	likely benign	24
24223	MLL2	rs1038705024	SNP	missense variant	L/F	3009	11	0.01	997	probably damaging	0.996	25001	likely benign	25
24224	MLL2	rs1478742796	SNP	missense variant	E/D	3008	1001	1	24	benign	0.023	11001	likely benign	11
24225	MLL2	rs137934366	SNP	missense variant	E/D	3007	201	0.2	13	benign	0.012	14001	likely benign	14
24226	MLL2	rs371231725	SNP	missense variant	K/R	3001	21	0.02	550	possibly damaging	0.549	25001	likely benign	25
24227	MLL2	rs898873941	SNP	missense variant	A/G	2999	381	0.38	472	possibly damaging	0.471	22001	likely benign	22
24228	MLL2	rs767902511	SNP	missense variant	A/S	2999	371	0.37	92	benign	0.091	18001	likely benign	18
24229	MLL2	rs1432465908	SNP	missense variant	D/V	2998	1	0	964	probably damaging	0.963	25001	likely benign	25
24230	MLL2	rs750793606	SNP	missense variant	F/C	2997	61	0.06	847	possibly damaging	0.846	24001	likely benign	24

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