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
4771	MAP2K4	rs1160578914	SNP	missense variant	I/T	243	1	0	992	probably damaging	0.991	27001	likely benign	27
4772	MAP2K4	rs1361335563	SNP	missense variant	V/L	255	1	0	747	possibly damaging	0.746	26001	likely benign	26
4773	MAP2K4	rs200798818	SNP	missense variant	A/S	264	1	0	996	probably damaging	0.995	28001	likely benign	28
4774	MAP2K4	rs76726054	SNP	missense variant	C/W	266	1	0	1001	probably damaging	1	27001	likely benign	27
4775	MAP2K4	rs1455763623	SNP	missense variant	P/A	277	1	0	910	probably damaging	0.909	25001	likely benign	25
4776	MAP2K4	rs753665559	SNP	missense variant	A/T	279	571	0.57	70	benign	0.069	23001	likely benign	23
4777	MAP2K4	rs1183392154	SNP	missense variant	A/V	279	291	0.29	66	benign	0.065	23001	likely benign	23
4778	MAP2K4	rs537815982	SNP	missense variant	V/I	286	311	0.31	100	benign	0.099	22001	likely benign	22
4779	MAP2K4	rs1334746981	SNP	missense variant	S/C	288	1	0	998	probably damaging	0.997	27001	likely benign	27
4780	MAP2K4	rs781002756	SNP	missense variant	A/S	301	141	0.14	840	possibly damaging	0.839	25001	likely benign	25

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