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
25281	MLL2	rs748193878	SNP	missense variant	K/R	1711	61	0.06	159	benign	0.158	22001	likely benign	22
25282	MLL2	rs587778457	SNP	missense variant	T/M	1710	311	0.31	1	benign	0	17001	likely benign	17
25283	MLL2	rs1331807800	SNP	missense variant	R/H	1709	11	0.01	998	probably damaging	0.997	27001	likely benign	27
25284	MLL2	rs1372083024	SNP	missense variant	R/C	1709	21	0.02	998	probably damaging	0.997	29001	likely benign	29
25285	MLL2	rs1372083024	SNP	missense variant	R/G	1709	31	0.03	998	probably damaging	0.997	26001	likely benign	26
25286	MLL2	rs771315206	SNP	missense variant	H/Q	1707	21	0.02	997	probably damaging	0.996	23001	likely benign	23
25287	MLL2	rs1024285765	SNP	missense variant	R/Q	1702	1	0	995	probably damaging	0.994	27001	likely benign	27
25288	MLL2	rs776929490	SNP	missense variant	G/S	1697	11	0.01	1000	probably damaging	0.999	28001	likely benign	28
25289	MLL2	rs780507577	SNP	missense variant	R/Q	1693	1	0	995	probably damaging	0.994	27001	likely benign	27
25290	MLL2	rs749841843	SNP	missense variant	Y/H	1692	1	0	998	probably damaging	0.997	27001	likely benign	27

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