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
21741	DNMT3A	rs376830288	SNP	missense variant	W/C	860	1	0	1001	probably damaging	1	32001	likely deleterious	32
21742	DNMT3A	rs373014701	SNP	missense variant	W/R	860	1	0	935	probably damaging	0.934	33001	likely deleterious	33
21743	DNMT3A	rs746967478	SNP	missense variant	M/V	852	31	0.03	108	benign	0.107	23001	likely benign	23
21744	DNMT3A	rs754780499	SNP	missense variant	V/G	850	1	0	996	probably damaging	0.995	29001	likely benign	29
21745	DNMT3A	rs749417012	SNP	missense variant	G/S	843	41	0.04	743	possibly damaging	0.742	26001	likely benign	26
21746	DNMT3A	rs771174392	SNP	missense variant	Q/R	842	31	0.03	994	probably damaging	0.993	27001	likely benign	27
21747	DNMT3A	rs1404111595	SNP	missense variant	K/E	841	1	0	695	possibly damaging	0.694	28001	likely benign	28
21748	DNMT3A	rs1167486470	SNP	missense variant	I/M	840	11	0.01	388	benign	0.387	22001	likely benign	22
21749	DNMT3A	rs994825529	SNP	missense variant	I/K	840	1	0	900	possibly damaging	0.899	28001	likely benign	28
21750	DNMT3A	rs961377711	SNP	missense variant	N/D	838	41	0.04	969	probably damaging	0.968	28001	likely benign	28

Left 2174 2175 2176